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7647-15-6 Usage

InChI:InChI=1/BrH.Na/h1H;/q;+1/p-1

7647-15-6 Well-known Company Product Price

Brand (Code)Product description CAS number Packaging Price Detail
Alfa Aesar (10860)  Sodium bromide, Puratronic?, 99.9955% (metals basis)    7647-15-6 25g 589.0CNY Detail
Alfa Aesar (10860)  Sodium bromide, Puratronic?, 99.9955% (metals basis)    7647-15-6 100g 2352.0CNY Detail
Alfa Aesar (39426)  Sodium bromide, ultra dry, 99.999% (metals basis)    7647-15-6 5g 828.0CNY Detail
Alfa Aesar (39426)  Sodium bromide, ultra dry, 99.999% (metals basis)    7647-15-6 25g 3017.0CNY Detail
Alfa Aesar (14037)  Sodium bromide, 97%    7647-15-6 500g 301.0CNY Detail
Alfa Aesar (14037)  Sodium bromide, 97%    7647-15-6 2kg 881.0CNY Detail
Alfa Aesar (87604)  Sodium bromide, 99.99% (metals basis)    7647-15-6 5g 529.0CNY Detail
Alfa Aesar (87604)  Sodium bromide, 99.99% (metals basis)    7647-15-6 25g 1667.0CNY Detail
Alfa Aesar (A10552)  Sodium bromide, 99+% (dry wt.), water <1.0%    7647-15-6 250g 249.0CNY Detail
Alfa Aesar (A10552)  Sodium bromide, 99+% (dry wt.), water <1.0%    7647-15-6 1000g 753.0CNY Detail
Alfa Aesar (A10552)  Sodium bromide, 99+% (dry wt.), water <1.0%    7647-15-6 5000g 1870.0CNY Detail
Alfa Aesar (36444)  Sodium bromide, ACS, 99.0% min    7647-15-6 500g 627.0CNY Detail

7647-15-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium bromide

1.2 Other means of identification

Product number -
Other names Sodiumbomide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7647-15-6 SDS

7647-15-6Synthetic route

(C8H13B(NH(CH2CH2CH2CH3))CH2NH(CH2CH2CH2CH3))(1+)*Br(1-) = (C8H13B(NH(CH2CH2CH2CH3)))CH2NH(CH2CH2CH2CH3)Br

(C8H13B(NH(CH2CH2CH2CH3))CH2NH(CH2CH2CH2CH3))(1+)*Br(1-) = (C8H13B(NH(CH2CH2CH2CH3)))CH2NH(CH2CH2CH2CH3)Br

sodium methylate
124-41-4

sodium methylate

A

3-methoxy-7-n-butylaminomethyl-3-boracyclo[3.3.1]-nonane
74775-97-6

3-methoxy-7-n-butylaminomethyl-3-boracyclo[3.3.1]-nonane

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In methanol (dry Ar); to the B-compound in MeOH added soln. of NaOCH3 in MeOH at 20°C; refluxed for 30 min; solvent removed in vacuo; ether added; NaBr filtered; washed with ether; ether sol. evapd. in vacuo; recrystd.; elem. anal.;A 66%
B 99.5%
Bromotriethylgermanium
1067-10-3

Bromotriethylgermanium

sodium 3,5-di-tert-butyl-o-benzosemiquinolate
4679-12-3, 61373-02-2

sodium 3,5-di-tert-butyl-o-benzosemiquinolate

A

3,5-di-tert-butyl-o-benzoquinone
3383-21-9

3,5-di-tert-butyl-o-benzoquinone

B

C6H2(C(CH3)3)2(OGe(C2H5)3)2
51639-37-3

C6H2(C(CH3)3)2(OGe(C2H5)3)2

C

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In tetrahydrofuran mixing of solns. (20°C); removal of THF (vavc.), addn. of hexane, pptn. and sepn. of NaBr (filtration off), crystn. of quinone (low temp.); (t-Bu)2C6H2(OGeEt3)2 in mother liquor not isolated; GLC;A 36%
B 47%
C 98%
bis(cyclopentadienyl)dibromozirconium

bis(cyclopentadienyl)dibromozirconium

sodium dimethyldithiocarbamate
128-04-1

sodium dimethyldithiocarbamate

A

bis(η5-cyclopentadienyl)bromo(N,N-dimethyldithiocarbamato)zirconium(IV)

bis(η5-cyclopentadienyl)bromo(N,N-dimethyldithiocarbamato)zirconium(IV)

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In dichloromethane Kinetics; Stirring of mixt. of starting complexes in CH2Cl2 at reflux under anhydrous conditions in a dry Ar atmosphere (24 h).; Filtn. of react. mixt., removal of solvent by trap-to-trap distn., crystn. of crude resulting material from CH2Cl2 under hexane, elem. anal., variable-temp. NMR spectroscopy.;A 98%
B n/a
3-methoxy-7-bromomethyl-3-borabicyclo[3.3.1]nonane
74789-86-9

3-methoxy-7-bromomethyl-3-borabicyclo[3.3.1]nonane

sodium methylate
124-41-4

sodium methylate

A

C8H13(CH2OCH3)B(OCH3)
74789-87-0

C8H13(CH2OCH3)B(OCH3)

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In methanol (dry Ar); heated for 1.5 h at 50°C; MeOH vac. distd.; residue treated isopentane; ppt. NaBr filtered; filtrate distn.; elem. anal.;A 84%
B 98%
aluminium bromide
7727-15-3

aluminium bromide

sodium triethoxysilanolate
53201-03-9

sodium triethoxysilanolate

A

tris(triethoxysiloxy)aluminum

tris(triethoxysiloxy)aluminum

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In benzene (glovebox); addn. of a soln. of AlBr3 in C6H6 to a soln. of silicon compd. in C6H6 in vac. with stirring, sealing, heating to 40°C for 30min with shaking; centrifugation, decantation, evapn; elem. anal.;A 98%
B 98%
diethylgermanium dibromide
13314-53-9

diethylgermanium dibromide

disodium 3,5-di-t-butyl-1,2-pyrocatecholate
4679-12-3, 61373-02-2

disodium 3,5-di-t-butyl-1,2-pyrocatecholate

A

2,2-diethyl(6,8-di-tert-butyl)-4,5-benzo-2-germa-1,3-dioxolane
78100-52-4

2,2-diethyl(6,8-di-tert-butyl)-4,5-benzo-2-germa-1,3-dioxolane

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In diethyl ether 3 h at 20°C; NaBr washed out (water); ether evapd.; recrystd. (acetonitrile); elem. anal.;A 87%
B 95%
1,3-Dibromohexafluoropropane
4259-29-4

1,3-Dibromohexafluoropropane

A

sodium perfluoropropane-1,3-di(sulfinate)

sodium perfluoropropane-1,3-di(sulfinate)

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
With sodium dithionite; sodium hydrogencarbonate In water; acetonitrile at 35 - 65℃; for 5.5h; Product distribution / selectivity;A 94%
B n/a
With disodium hydrogenphosphate; sodium dithionite In water; acetonitrile at 35 - 65℃; Product distribution / selectivity;A 84%
B n/a
sodium dicarbonyl(cyclopentadienyl)ferrate

sodium dicarbonyl(cyclopentadienyl)ferrate

triisopropylgermylmercuric bromide
105260-39-7

triisopropylgermylmercuric bromide

A

{(η-cyclopentadienyl)Fe(CO)2}2Hg

{(η-cyclopentadienyl)Fe(CO)2}2Hg

B

bis(triisopropylgermyl)mercury
24004-54-4

bis(triisopropylgermyl)mercury

C

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In tetrahydrofuran; hexane addn. of Na-compound (prepared from (C5H5)Fe(CO)3 and excess 3% Na-amalgam) in THF to i-Pr3GeHgBr (prepared from (i-PrGe)2Hg and Br2) in hexane at -40°C; pptn. (NaBr), replacing of solvents in the mother-liquor by hexane, pptn. of Fe-compound, isolation of (i-Pr3Ge)2Hg by fractionation of the soln. in vac.;A 90%
B 93%
C 71%
sodium tetrahydroborate
16940-66-2

sodium tetrahydroborate

lithium bromide
7550-35-8

lithium bromide

A

lithium borohydride

lithium borohydride

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
With 1,3-dioxolane In further solvent(s) (N2); salts mixt. (1/1 molar ratio) stirred at 25-74°C for 1-48 h in 1,3-dioxolane; heated (vac.);A 92%
B n/a
With 1,2-dimethoxyethane In 1,2-dimethoxyethane (N2); salts mixt. (1/1 molar ratio) stirred at 25-85°C for 1-36 h in monoglyme; heated (vac.);A >99
B n/a
With C4H8O In tetrahydrofuran (N2); salts mixt. (1/1 molar ratio) stirred at 25-67°C for 1-48 h in THF; heated (vac.);
With diethyl ether In diethyl ether (N2); salts mixt. (1/1 molar ratio) stirred at 25-35°C for 1-32 h in Et2O; heated (vac.);A 6-100
B n/a
diethylgermanium dibromide
13314-53-9

diethylgermanium dibromide

sodium 3,5-di-tert-butyl-o-benzosemiquinolate
4679-12-3, 61373-02-2

sodium 3,5-di-tert-butyl-o-benzosemiquinolate

A

2,2-diethyl(6,8-di-tert-butyl)-4,5-benzo-2-germa-1,3-dioxolane
78100-52-4

2,2-diethyl(6,8-di-tert-butyl)-4,5-benzo-2-germa-1,3-dioxolane

B

3,5-di-tert-butyl-o-benzoquinone
3383-21-9

3,5-di-tert-butyl-o-benzoquinone

C

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In diethyl ether Na-:Ge-compound 2:1, 3 h at 20°C; ether replaced with hexane; NaBr washed out (water); recrystd. (acetonitrile);A 69%
B 87%
C 92%
picoline
108-89-4

picoline

indium tribromide
13465-09-3

indium tribromide

sodium 3,5-di-tert-butyl-o-benzosemiquinolate
4679-12-3, 61373-02-2

sodium 3,5-di-tert-butyl-o-benzosemiquinolate

A

[InBr(((CH3)3C)2C6H2O2)(C5H5N)2]*C4H8O

[InBr(((CH3)3C)2C6H2O2)(C5H5N)2]*C4H8O

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In tetrahydrofuran byproducts: H2; N2, blue soln. of semiquinone sodium salt added dropwise over 1 h to a soln. of In-salt, stirred for 2 h at room temp., NaBr removed from intermediate product by filtrn., excess 4-picoline added to the filtrate; collected, dried, recrystd. (toluene/THF); elem. anal.; intermediate and formn. of In(I) products also discussed;A 50%
B 92%
sodium hypobromide

sodium hypobromide

urea
57-13-6

urea

A

carbon dioxide
124-38-9

carbon dioxide

B

nitrogen
7727-37-9

nitrogen

C

water
7732-18-5

water

D

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
A 90%
B 90%
C 90%
D 90%
Bromotriethylgermanium
1067-10-3

Bromotriethylgermanium

sodium 3,5-di-tert-butyl-o-benzosemiquinolate
4679-12-3, 61373-02-2

sodium 3,5-di-tert-butyl-o-benzosemiquinolate

A

2,2-diethyl(6,8-di-tert-butyl)-4,5-benzo-2-germa-1,3-dioxolane
78100-52-4

2,2-diethyl(6,8-di-tert-butyl)-4,5-benzo-2-germa-1,3-dioxolane

B

3,5-di-tert-butyl-o-benzoquinone
3383-21-9

3,5-di-tert-butyl-o-benzoquinone

C

C6H2(C(CH3)3)2(OGe(C2H5)3)2
51639-37-3

C6H2(C(CH3)3)2(OGe(C2H5)3)2

D

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In diethyl ether 3 h at 20°C; ether replaced with hexane; NaBr washed out (water); recrystd. (hexane);A 12%
B 63%
C 88%
D 90%
sodium ethanolate
141-52-6

sodium ethanolate

methyldibromobismuth(III)
60458-17-5

methyldibromobismuth(III)

2-hydroxyethanethiol
60-24-2

2-hydroxyethanethiol

A

CH3Bi(SCH2CH2OH)2
60458-10-8

CH3Bi(SCH2CH2OH)2

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
20°C, equiv. amt. of HSCH2C6H5; NaCl filtered off, the solvent evapd. in vac.;A 88%
B n/a
sodium ethanolate
141-52-6

sodium ethanolate

methyldibromobismuth(III)
60458-17-5

methyldibromobismuth(III)

A

methyldiethoxybismutane
60458-07-3

methyldiethoxybismutane

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In ethanol abs. ethanol, 24 h, -25°C;A 87%
B n/a
sodium tetrafluoroborate
13755-29-8

sodium tetrafluoroborate

C14H16NO2(1+)*Br(1-)

C14H16NO2(1+)*Br(1-)

A

C14H16NO2(1+)*BF4(1-)

C14H16NO2(1+)*BF4(1-)

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In water at 20℃; for 1h;A 87%
B n/a
1,4-dibromo-1,1,2,2,3,3,4,4-octafluoro-butane
335-48-8

1,4-dibromo-1,1,2,2,3,3,4,4-octafluoro-butane

A

sodium perfluorobutane-1,4-di(sulfinate)

sodium perfluorobutane-1,4-di(sulfinate)

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
With sodium dithionite; sodium hydrogencarbonate In water; acetonitrile at 35 - 65℃; for 6h; Product distribution / selectivity;A 86%
B n/a
sodium ethanolate
141-52-6

sodium ethanolate

methyldibromobismuth(III)
60458-17-5

methyldibromobismuth(III)

phenylmethanethiol
100-53-8

phenylmethanethiol

A

Bis-(benzylthio)-methylbismutin
60458-09-5

Bis-(benzylthio)-methylbismutin

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
20°C, equiv. amt. of HSCH2C6H5; NaCl filtered off, the solvent evapd. in vac.;A 83%
B n/a
sodium ethanolate
141-52-6

sodium ethanolate

methyldibromobismuth(III)
60458-17-5

methyldibromobismuth(III)

thiophenol
108-98-5

thiophenol

A

Methyl-bis-(phenylthio)-bismutin
28609-60-1

Methyl-bis-(phenylthio)-bismutin

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
20°C, equiv. amt. of thiophenol; NaCl filtered off, the solvent evapd. in vac.;A 80%
B n/a
sodium tetrafluoroborate
13755-29-8

sodium tetrafluoroborate

C13H14NO(1+)*Br(1-)

C13H14NO(1+)*Br(1-)

A

C13H14NO(1+)*BF4(1-)

C13H14NO(1+)*BF4(1-)

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In water at 20℃; for 1h;A 80%
B n/a
sodium{(THF)2.3} hexacarbonylniobate
15602-39-8

sodium{(THF)2.3} hexacarbonylniobate

Pyridine hydrobromide
18820-82-1

Pyridine hydrobromide

A

tetracarbonyl{1,2-bis(diphenylphosphino)ethane}bromoniobium
112713-60-7

tetracarbonyl{1,2-bis(diphenylphosphino)ethane}bromoniobium

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
With C2H4(P(C6H5)2)2 In tetrahydrofuran; toluene byproducts: C5H5N, CO, H2; Treating of suspn. of diphos and (H-py)Br in THF with Nb-complex at room temp. under a CO atmosphere.; Immediate react. with evolution of CO and H2 (gas chromy.) obsd. Stirring (2 h, room temp.), removal of THF (vac., room temp.), dissolving of residue (toluene, CO), stirring (2 h), filtn., treating with n-heptane. Sepn. of microcryst., elem. anal.;A 78%
B n/a
1,4-bis(bromomethyl)benzene
623-24-5

1,4-bis(bromomethyl)benzene

Na[CpMo(CO)3]
12107-35-6

Na[CpMo(CO)3]

A

(Mo(C5H5)(CO)3)CH2C6H4CH2((CO)3(C5H5)Mo)

(Mo(C5H5)(CO)3)CH2C6H4CH2((CO)3(C5H5)Mo)

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In tetrahydrofuran A mixt. of BrCH2C6H4CH2Br and Na(MO(cp)(CO)3) in THF is stirred at roomtemp. for 1.5 h.; The soln. is filtered to remove NaBr, concd. in vacuo and treated with methanol to give yellow crystals of (Mo(cp)(CO)3)CH2C6H4CH2((CO)3(cp)Mo);A 76%
B n/a
2Na(1+)*Ru2(CO)8(2-)=Na2{Ru2(CO)8}

2Na(1+)*Ru2(CO)8(2-)=Na2{Ru2(CO)8}

tetraphenylphosphonium bromide
2751-90-8

tetraphenylphosphonium bromide

2P(C6H5)4(1+)*Ru2(CO)8(2-)=(P(C6H5)4)2{Ru2(CO)8}

2P(C6H5)4(1+)*Ru2(CO)8(2-)=(P(C6H5)4)2{Ru2(CO)8}

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In tetrahydrofuran inert atmosphere; stirring (room temp., 4 h, pptn.); filtration, washing (THF), extn. (MeCN), partial evapn. of CH3CN soln., pptn. on Et2O addn., washing (Et2O), drying (vac., 1 h); elem. anal.;A 75%
B n/a
2Na(1+)*Os2(CO)8(2-)=Na2{Os2(CO)8}

2Na(1+)*Os2(CO)8(2-)=Na2{Os2(CO)8}

tetraphenylphosphonium bromide
2751-90-8

tetraphenylphosphonium bromide

2P(C6H5)4(1+)*Os2(CO)8(2-)=(P(C6H5)4)2{Os2(CO)8}

2P(C6H5)4(1+)*Os2(CO)8(2-)=(P(C6H5)4)2{Os2(CO)8}

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In tetrahydrofuran inert atmosphere; stirring (room temp., 4 h, pptn.); filtration, washing (THF), extn. (MeCN), partial evapn. of CH3CN soln., pptn. on Et2O addn., washing (Et2O), drying (vac., 1 h);A 74%
B n/a
2Na(1+)*FeRu(CO)8(2-)=Na2{FeRu(CO)8}

2Na(1+)*FeRu(CO)8(2-)=Na2{FeRu(CO)8}

tetraphenylphosphonium bromide
2751-90-8

tetraphenylphosphonium bromide

2P(C6H5)4(1+)*FeRu(CO)8(2-)=(P(C6H5)4)2{FeRu(CO)8}

2P(C6H5)4(1+)*FeRu(CO)8(2-)=(P(C6H5)4)2{FeRu(CO)8}

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In tetrahydrofuran inert atmosphere; stirring (room temp., 4 h, pptn.); filtration, washing (THF), extn. (MeCN), partial evapn. of CH3CN soln., pptn. on Et2O addn., washing (Et2O), drying (vac., 1 h); elem. anal.;A 71%
B n/a
picoline
108-89-4

picoline

HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCoBr2
115381-20-9

HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCoBr2

sodium perchlorate

sodium perchlorate

HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCo(NC5H4CH3)Br(1+)*ClO4(1-)=[HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCo(NC5H4CH3)Br]ClO4
256460-68-1

HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCo(NC5H4CH3)Br(1+)*ClO4(1-)=[HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCo(NC5H4CH3)Br]ClO4

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In methanol; water addn. of satd. aq. soln. of NaClO4 to hot suspn. of Co complex in MeOH, addn. of stoichiom. amt. of substituted pyridine in MeOH (stirring), refluxing (water bath, 4 h), pptn. on volume reduction and standing (35°, 2 h); filtration, washing (cold water, MeOH, Et2O), drying (vac.); elem. anal.;A 69.7%
B n/a
2,6-Diaminopyridine
141-86-6

2,6-Diaminopyridine

HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCoBr2
115381-20-9

HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCoBr2

sodium perchlorate

sodium perchlorate

HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCo(N3C5H7)Br(1+)*ClO4(1-)=[HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCo(N3C5H7)Br]ClO4
256460-77-2

HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCo(N3C5H7)Br(1+)*ClO4(1-)=[HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCo(N3C5H7)Br]ClO4

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In methanol; water addn. of satd. aq. soln. of NaClO4 to hot suspn. of Co complex in MeOH, addn. of stoichiom. amt. of substituted pyridine in MeOH (stirring), refluxing (water bath, 4 h), pptn. on volume reduction and standing (35°, 2 h); filtration, washing (cold water, MeOH, Et2O), drying (vac.); elem. anal.;A 69.5%
B n/a
α-picoline
109-06-8

α-picoline

HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCoBr2
115381-20-9

HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCoBr2

sodium perchlorate

sodium perchlorate

HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCo(NC5H4CH3)Br(1+)*ClO4(1-)=[HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCo(NC5H4CH3)Br]ClO4
256460-65-8

HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCo(NC5H4CH3)Br(1+)*ClO4(1-)=[HONC(CH3)C(CH3)NOCH2ONC(CH3)C(CH3)NOCo(NC5H4CH3)Br]ClO4

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
In methanol; water addn. of satd. aq. soln. of NaClO4 to hot suspn. of Co complex in MeOH, addn. of stoichiom. amt. of substituted pyridine in MeOH (stirring), refluxing (water bath, 4 h), pptn. on volume reduction and standing (35°, 2 h); filtration, washing (cold water, MeOH, Et2O), drying (vac.); elem. anal.;A 67.9%
B n/a
sodium ethanolate
141-52-6

sodium ethanolate

methyldibromobismuth(III)
60458-17-5

methyldibromobismuth(III)

ethanethiol
75-08-1

ethanethiol

A

Methyldi(ethylthio)bismutan
60458-08-4

Methyldi(ethylthio)bismutan

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
20°C, equiv. amt. of C2H5SH; NaCl filtered off, the solvent evapd.in vac.;A 67%
B n/a
sodium hexacarbonyltantalate*THF
15602-40-1

sodium hexacarbonyltantalate*THF

Pyridine hydrobromide
18820-82-1

Pyridine hydrobromide

A

tetracarbonyl{1,2-bis(diphenylphosphino)ethane}bromotantalum
112713-59-4

tetracarbonyl{1,2-bis(diphenylphosphino)ethane}bromotantalum

B

sodium bromide
7647-15-6

sodium bromide

Conditions
ConditionsYield
With C2H4(P(C6H5)2)2 In tetrahydrofuran; toluene byproducts: C5H5N, CO, H2; Treating of suspn. of diphos and (H-py)Br in THF with Ta-complex at room temp. under a CO atmosphere.; Immediate react. with evolution of CO and H2 (gas chromy.) obsd. Stirring (2 h, room temp.), removal of THF (vac., room temp.), dissolving of residue (toluene, CO), stirring (2 h), filtn., treating with n-heptane. Sepn. of microcryst., elem. anal.;A 66%
B n/a
ammonium perrhenate

ammonium perrhenate

sodium bromide
7647-15-6

sodium bromide

rhenium(VI) tetrabromide oxide
23601-08-3

rhenium(VI) tetrabromide oxide

Conditions
ConditionsYield
In sulfuric acid NaBr addn. to NH4ReO4 soln. in concd. H2SO4 (crystn.); extn. (toluene), distn. off of toluene; elem. anal.;100%
In sulfuric acid byproducts: HBr, Br2; dissoln. of NH4ReO4 in 98% H2SO4, dropwise addn. of 20-50 fold excess NaBr, stirring (20-30 min); other alkali metal bromides can be used instead of NaBr; extn. (toluene), distn. off of solvent (vac., room temp.); elem. anal.;99%
(1-hexadecyl-1,4,8,11,-tetra-azacyclotetradecane)nickel(II) perchlorate

(1-hexadecyl-1,4,8,11,-tetra-azacyclotetradecane)nickel(II) perchlorate

sodium bromide
7647-15-6

sodium bromide

(1-hexadecyl-1,4,8,11,-tetra-azacyclotetradecane)nickel(II) bromide
128026-89-1, 128058-84-4

(1-hexadecyl-1,4,8,11,-tetra-azacyclotetradecane)nickel(II) bromide

Conditions
ConditionsYield
In dichloromethane; water A CH2Cl2 layer of Ni(HNC2H4NHC3H6NHC2H4N(C16H33)C3H6)(ClO4)2 is equilibrated with an aq. layer of NaBr.; The ClO4(1-) ions are quantitatively replaced by the I(1-) ions forming the complex Ni(HNC2H4NHC3H6NHC2H4N(C16H33)C3H6)Br2.;100%
chloro{2-(dimethylaminomethyl)phenyl}phenylbismuthine
721944-47-4

chloro{2-(dimethylaminomethyl)phenyl}phenylbismuthine

sodium bromide
7647-15-6

sodium bromide

bromo{2-(dimethylaminomethyl)phenyl}phenylbismuthine
721944-48-5

bromo{2-(dimethylaminomethyl)phenyl}phenylbismuthine

Conditions
ConditionsYield
In water; benzene Ar; NaBr in water added to Cl(C6H4CH2N(CH3)2)Bi(C6H5)Cl in benzene; organic layer extd. with ethyl acetate; ext. evapd. under reduced pressure; crystn. from hexane/CH2Cl2 gave crystals;100%
[Pt(OH)(P(C6H11)3)(CH2C6H5)]2

[Pt(OH)(P(C6H11)3)(CH2C6H5)]2

sodium bromide
7647-15-6

sodium bromide

[Pt(Br)(P(C6H11)3)(CH2C6H5)]2
158640-92-7

[Pt(Br)(P(C6H11)3)(CH2C6H5)]2

Conditions
ConditionsYield
With tetrafluoroboric acid In water; toluene under Ar; a soln. of the starting complex in toluene is added to NaBr in aq. HBF4, mixt. stirred for 30 min; the toluene layer is separated, evapd.; the solid is treated with water-toluene, the organic layer is separated, evapd.; the residue is dissolved in toluene, hexane is added; elem. anal.;100%
PdCl2((C4H9)2C3H3N2(CH2C6H5)2)2

PdCl2((C4H9)2C3H3N2(CH2C6H5)2)2

PdClBr((C4H9)2C3H3N2(CH2C6H5)2)2

PdClBr((C4H9)2C3H3N2(CH2C6H5)2)2

sodium bromide
7647-15-6

sodium bromide

PdBr2((C4H9)2C3H3N2(CH2C6H5)2)2

PdBr2((C4H9)2C3H3N2(CH2C6H5)2)2

Conditions
ConditionsYield
In N,N-dimethyl-formamide mixt. of Pd-complexes and NaBr in DMF was stirred for 12 h at 120°C under Ar, cooled to ambient temp.; diluted with Et2O, washed with H2O, dried over MgSO4, filtered, concd., silica gel with cyclohexane/AcOEt; elem. anal.;100%
palladium(II) meso-anthriporphyrin-Cl

palladium(II) meso-anthriporphyrin-Cl

sodium bromide
7647-15-6

sodium bromide

palladium(II) meso-anthriporphyrin-Br

palladium(II) meso-anthriporphyrin-Br

Conditions
ConditionsYield
With AgBF4 In methanol; dichloromethane100%
[(2,6-bis-(di-tert-butylphosphinomethyl)pyridine)Rh(acetone)][BF4]

[(2,6-bis-(di-tert-butylphosphinomethyl)pyridine)Rh(acetone)][BF4]

sodium bromide
7647-15-6

sodium bromide

[(2,6-bis-(di-tert-butylphosphinomethyl)pyridine)RhBr]
1447423-46-2

[(2,6-bis-(di-tert-butylphosphinomethyl)pyridine)RhBr]

Conditions
ConditionsYield
In acetone at 20℃; for 1h; Inert atmosphere; Schlenk technique; Glovebox;100%
cis-dichlorobis(diphenylvinylphosphine)palladium(II)
113214-83-8

cis-dichlorobis(diphenylvinylphosphine)palladium(II)

sodium bromide
7647-15-6

sodium bromide

trans-dibromobis(diphenylvinylphosphine)palladium(II)
113214-84-9

trans-dibromobis(diphenylvinylphosphine)palladium(II)

Conditions
ConditionsYield
In methanol; dichloromethane; water Addn. of a CH3OH/H2O soln. of NaBr to a CH2Cl2 soln. of dichlorobis(diphenylvinylphosphine)palladium(II).; Elem.anal.;99.5%
[PtClMe(2,9-dimethyl-1,10-phenanthroline)(CH2=CHOH)]
198629-52-6

[PtClMe(2,9-dimethyl-1,10-phenanthroline)(CH2=CHOH)]

sodium bromide
7647-15-6

sodium bromide

[PtBrMe(2,9-dimethyl-1,10-phenanthroline)(CH2=CHOH)]
198629-59-3

[PtBrMe(2,9-dimethyl-1,10-phenanthroline)(CH2=CHOH)]

Conditions
ConditionsYield
In chloroform slight excess of NaBr, stirring at room temp. for 1 h; sepn. of org. layer, washing (water), filtration over Na2SO4, solvent removal (vac.);99%
chloro[bis(2-diphenylphosphinophenyl)amide]nickel(II)
579490-55-4

chloro[bis(2-diphenylphosphinophenyl)amide]nickel(II)

sodium bromide
7647-15-6

sodium bromide

[N(o-C6H4PPh2)2]NiBr
881020-83-3

[N(o-C6H4PPh2)2]NiBr

Conditions
ConditionsYield
In acetone under N2 atm. suspn. NaBr in acetone was added to soln. Ni complex in acetone and stirred at room temp. for 24 h; react. mixt. was evapd. to dryness in vacuo, residue was extd. with CH2Cl2, filtered through Celite, and evapd. in vacuo; elem. anal.;99%
Cr(3+)*NCS(1-)*5(NH3)*2NO3(1-)={CrSCN(NH3)5}(NO3)2

Cr(3+)*NCS(1-)*5(NH3)*2NO3(1-)={CrSCN(NH3)5}(NO3)2

sodium bromide
7647-15-6

sodium bromide

Cr(3+)*5NH3*NCS(1-)*2Br(1-)=[Cr(NH3)5(NCS)]Br2

Cr(3+)*5NH3*NCS(1-)*2Br(1-)=[Cr(NH3)5(NCS)]Br2

Conditions
ConditionsYield
In not given dissoln. of Cr-complex in 0.01 M HCl (30°C), pptn. on addn. of satd. NaBr and slow cooling to 0°C; elem. anal.;99%
ferrocenium hexafluorophosphate

ferrocenium hexafluorophosphate

[Mo2Rh2((t)BuNC)4(6-diphenylphosphino-2-pyridonate)4](Cl)2

[Mo2Rh2((t)BuNC)4(6-diphenylphosphino-2-pyridonate)4](Cl)2

sodium bromide
7647-15-6

sodium bromide

[Mo2Rh2(Br)2((t)BuNC)4(6-diphenylphosphino-2-pyridonate)4](PF6)2

[Mo2Rh2(Br)2((t)BuNC)4(6-diphenylphosphino-2-pyridonate)4](PF6)2

Conditions
ConditionsYield
In dichloromethane 1) NaBr (excess), 2) (Cp2Fe)PF6 (2 equiv), room temp.;99%
(S(Ru),R(C))-{Ru(η5-C5H5)(Cl)(prophos)}

(S(Ru),R(C))-{Ru(η5-C5H5)(Cl)(prophos)}

(R(Ru),R(C))-{Ru(η5-C5H5)(Cl)(prophos)}

(R(Ru),R(C))-{Ru(η5-C5H5)(Cl)(prophos)}

sodium bromide
7647-15-6

sodium bromide

[CpRuBr((R)-1,2-bis(diphenylphosphanyl)propane)]

[CpRuBr((R)-1,2-bis(diphenylphosphanyl)propane)]

Conditions
ConditionsYield
In methanol addn. of NaBr to methanolic soln. of ruthenium compd., heating at 50°C for 20 h; NMR;99%
[Pd(C6H2(CH2SPh)-2,6-(OH)-4)(MeCN)]BF4
1070260-80-8

[Pd(C6H2(CH2SPh)-2,6-(OH)-4)(MeCN)]BF4

sodium bromide
7647-15-6

sodium bromide

[PdBr(C6H2(CH2SPh)-2,6-(OH)-4)]
1070260-64-8

[PdBr(C6H2(CH2SPh)-2,6-(OH)-4)]

Conditions
ConditionsYield
In water; acetonitrile (under N2, Schlenk); aq. soln. of NaBr added to MeCN soln. of Pd-complex, stirred for 2 h at ambient temp.; concd. to removed volatiles, residue washed with H2O, dried in vacuo; elem. anal.;99%
((CH2)3CH3)4C8H2N4(RuCl2CH3C6H4CH(CH3)2)2*0.25CH2Cl2

((CH2)3CH3)4C8H2N4(RuCl2CH3C6H4CH(CH3)2)2*0.25CH2Cl2

sodium bromide
7647-15-6

sodium bromide

((CH2)3CH3)4C8H2N4(RuBr2CH3C6H4CH(CH3)2)2

((CH2)3CH3)4C8H2N4(RuBr2CH3C6H4CH(CH3)2)2

Conditions
ConditionsYield
In dichloromethane; acetone (under Ar, Schlenk); NaBr added to soln. of Ru-complex in CH2Cl2-acetone1:1, stirred for 4 h at room temp.; volatiles evapd., silica column chromy. with CH2Cl2-acetone 95:5, recrystd. from CH2Cl2-pentane at -20°C; elem. anal.;99%
pyridine
110-86-1

pyridine

(S)-4-benzyl-3-(biphenyl-4-ylmethyl)-1-(2,6-diisopropylphenyl)-4,5-dihydro-1H-imidazol-3-ium bromide
1450713-40-2

(S)-4-benzyl-3-(biphenyl-4-ylmethyl)-1-(2,6-diisopropylphenyl)-4,5-dihydro-1H-imidazol-3-ium bromide

sodium bromide
7647-15-6

sodium bromide

palladium dichloride

palladium dichloride

Pd[(S)-4-benzyl-3-(biphenyl-4-ylmethyl)-1-(2,6-diisopropylphenyl)imidazolin-2-ylidene](pyridine)Br2

Pd[(S)-4-benzyl-3-(biphenyl-4-ylmethyl)-1-(2,6-diisopropylphenyl)imidazolin-2-ylidene](pyridine)Br2

Conditions
ConditionsYield
With potassium carbonate at 80℃; for 12h; Inert atmosphere;99%
3-butyl-1-isopropyl-1H-benzo[d]imidazol-3-ium bromide

3-butyl-1-isopropyl-1H-benzo[d]imidazol-3-ium bromide

palladium diacetate
3375-31-3

palladium diacetate

sodium bromide
7647-15-6

sodium bromide

di-μ-bromo-bis(1-butyl-3-isopropylbenzimidazolin-2-ylidene)dibromodipalladium(II)

di-μ-bromo-bis(1-butyl-3-isopropylbenzimidazolin-2-ylidene)dibromodipalladium(II)

Conditions
ConditionsYield
In dimethyl sulfoxide at 90℃;99%
C14H22N2

C14H22N2

palladium diacetate
3375-31-3

palladium diacetate

sodium bromide
7647-15-6

sodium bromide

di-μ-bromo-bis(1-butyl-3-isopropylbenzimidazolin-2-ylidene)dibromodipalladium(II)

di-μ-bromo-bis(1-butyl-3-isopropylbenzimidazolin-2-ylidene)dibromodipalladium(II)

Conditions
ConditionsYield
In dimethyl sulfoxide at 90℃;99%
nickel(II) perchlorate hexahydrate

nickel(II) perchlorate hexahydrate

2,6-bis[N-(N-(carboxylmethyl)-N-((1-methylimidazol)methyl)amine)methyl]-4-methylphenolate, trisodium salt

2,6-bis[N-(N-(carboxylmethyl)-N-((1-methylimidazol)methyl)amine)methyl]-4-methylphenolate, trisodium salt

sodium acetate
127-09-3

sodium acetate

sodium bromide
7647-15-6

sodium bromide

Na1.5[Ni2(2,6-bis[N-(N-carboxymethyl-N-((1-methylimidazol-2-yl)methyl)amine)methyl]-4-methylphenolate)(acetato)2]Br0.5

Na1.5[Ni2(2,6-bis[N-(N-carboxymethyl-N-((1-methylimidazol-2-yl)methyl)amine)methyl]-4-methylphenolate)(acetato)2]Br0.5

Conditions
ConditionsYield
In methanol Ni-salt in methanol was added to a soln. of phenolate in methanol, Na-acetate and NaBr in methanol was added; pptn. with diethyl ether, filtered off, dried;98%
[(pentamethylcyclopentadienyl)((+)-2-N-[(S)-1-phenylethyl]pyrrolcarbaldiminate)chlororhodium]

[(pentamethylcyclopentadienyl)((+)-2-N-[(S)-1-phenylethyl]pyrrolcarbaldiminate)chlororhodium]

sodium bromide
7647-15-6

sodium bromide

[(pentamethylcyclopentadienyl)((+)-2-N-[(S)-1-phenylethyl]pyrrolcarbaldiminate)bromorhodium]

[(pentamethylcyclopentadienyl)((+)-2-N-[(S)-1-phenylethyl]pyrrolcarbaldiminate)bromorhodium]

Conditions
ConditionsYield
In methanol N2, an excess of Na compd., stirred for 1 h at room temp., solvent removed, residue dissolved (CH2Cl2), filtered (celite), solvent removed (repeated 3 times); elem. anal.;98%
cis-PtCl2[Ph2PNH(C6H3(3,5-CO2Me)2)](Ph2POMe)
1356935-23-3

cis-PtCl2[Ph2PNH(C6H3(3,5-CO2Me)2)](Ph2POMe)

sodium bromide
7647-15-6

sodium bromide

cis-PtBr2[Ph2PNH(C6H3(3,5-CO2Me)2)](Ph2POMe)
1356935-26-6

cis-PtBr2[Ph2PNH(C6H3(3,5-CO2Me)2)](Ph2POMe)

Conditions
ConditionsYield
In methanol; acetone Schlenk techniques; room temp.; elem. anal.;98%
1-benzyl-3-isopropyl-benzimidazolium bromide
1026780-30-2

1-benzyl-3-isopropyl-benzimidazolium bromide

palladium diacetate
3375-31-3

palladium diacetate

sodium bromide
7647-15-6

sodium bromide

di-μ-bromo-bis(1-benzyl-3-isopropylbenzimidazolin-2-ylidene)dibromodipalladium(II)

di-μ-bromo-bis(1-benzyl-3-isopropylbenzimidazolin-2-ylidene)dibromodipalladium(II)

Conditions
ConditionsYield
In dimethyl sulfoxide at 90℃;98%
C6H4N2CH(CH2CH2CH2CH3)(CH2C6H5)(1+)*I(1-)=C6H4N2CH(CH2CH2CH2CH3)(CH2C6H5)I
1315478-57-9

C6H4N2CH(CH2CH2CH2CH3)(CH2C6H5)(1+)*I(1-)=C6H4N2CH(CH2CH2CH2CH3)(CH2C6H5)I

palladium diacetate
3375-31-3

palladium diacetate

sodium bromide
7647-15-6

sodium bromide

di-μ-bromo-bis(1-benzyl-3-isopropylbenzimidazolin-2-ylidene)dibromodipalladium(II)

di-μ-bromo-bis(1-benzyl-3-isopropylbenzimidazolin-2-ylidene)dibromodipalladium(II)

Conditions
ConditionsYield
In dimethyl sulfoxide at 90℃;98%
dichlorobis(diphenylvinylphosphine)platinum(II)
98651-97-9, 114030-80-7

dichlorobis(diphenylvinylphosphine)platinum(II)

sodium bromide
7647-15-6

sodium bromide

dibromobis(diphenylvinylphosphine)platinum(II)
118207-85-5, 130324-15-1, 122170-80-3

dibromobis(diphenylvinylphosphine)platinum(II)

Conditions
ConditionsYield
In methanol; dichloromethane; water metathesis of chloride complex in CH2Cl2/CH3OH/H2O for 3 days with a mixture of NaBr and complex in 6:1 molar ratio under N2; elem. anal.;97.8%
rhodium(III) κC,κN,κN'-bis(N-tert-butyl)isophthalaldimin-2-yl dichloride
777855-06-8

rhodium(III) κC,κN,κN'-bis(N-tert-butyl)isophthalaldimin-2-yl dichloride

rhodium(III) κC,κN,κN'-bis(N-tert-butyl)isophthalaldimin-2-yl chloride bromide
777855-07-9

rhodium(III) κC,κN,κN'-bis(N-tert-butyl)isophthalaldimin-2-yl chloride bromide

sodium bromide
7647-15-6

sodium bromide

rhodium(III) κC,κN,κN'-bis(N-tert-butyl)isophthalaldimin-2-yl dibromide
777855-08-0

rhodium(III) κC,κN,κN'-bis(N-tert-butyl)isophthalaldimin-2-yl dibromide

Conditions
ConditionsYield
In acetone under N2; addn. of NaBr to mixt. of rhodium complexes in acetone, stirring overnight, evapn., extn. with chloroform, evapn., react. with NaBr, concn., stored on air for 3 d; ppt.; elem. anal.;97%

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