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762-75-4 Usage

General Description

tert-Butyl formate was one of the byproducts of methyl tert-butyl ether (MTBE) degradation.

Check Digit Verification of cas no

The CAS Registry Mumber 762-75-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 762-75:
(5*7)+(4*6)+(3*2)+(2*7)+(1*5)=84
84 % 10 = 4
So 762-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O2/c1-5(2,3)7-4-6/h4H,1-3H3

762-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl formate

1.2 Other means of identification

Product number -
Other names TERT-BUTYL FORMATE

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:762-75-4 SDS

762-75-4Synthetic route

2-oxopyridine-1(2H)-carbaldehyde
74885-84-0

2-oxopyridine-1(2H)-carbaldehyde

tert-butyl alcohol
75-65-0

tert-butyl alcohol

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
In dichloromethane at 40℃; for 72h;94%
1-Formyl-4(1H)-pyridinon
74885-83-9

1-Formyl-4(1H)-pyridinon

tert-butyl alcohol
75-65-0

tert-butyl alcohol

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
In dichloromethane for 144h; Ambient temperature;92%
formic acid
64-18-6

formic acid

tert-butyl alcohol
75-65-0

tert-butyl alcohol

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With silica triflate In hexane for 0.05h; Heating;90%
With sulfuric acid; silica gel In hexane for 0.583333h; Heating;85%
With aminopropylated mesoporous SBA-15 silica at 40℃; for 0.5h; Neat (no solvent); chemoselective reaction;80%
D-Val-OH
640-68-6

D-Val-OH

di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
89%
89%
89%
trans-1-benzyloxycarbonyl-3-aminomethyl-4-trifluoromethylpyrrolidine

trans-1-benzyloxycarbonyl-3-aminomethyl-4-trifluoromethylpyrrolidine

di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
In dichloromethane75.8%
tertiary butyl chloride
507-20-0

tertiary butyl chloride

carbon dioxide
124-38-9

carbon dioxide

A

tert-butyl formate
762-75-4

tert-butyl formate

B

tert-butyl alcohol
75-65-0

tert-butyl alcohol

Conditions
ConditionsYield
With hydrogen; sodium hydrogencarbonate; {W(CO)5Cl}(1-) In tetrahydrofuran at 150℃; under 80 - 85 Torr; for 24h;A 73.3%
B 26.7%
methanol
67-56-1

methanol

tert-butyl alcohol
75-65-0

tert-butyl alcohol

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With [bis({2‐[bis(propan‐2‐yl)phosphanyl]ethyl})amine](borohydride)(carbonyl)(hydride)iron(II); methacrylic acid methyl ester In toluene at 140℃; under 13689.1 Torr; for 8h; Reagent/catalyst; Autoclave; Inert atmosphere;71%
di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In 1,4-dioxane; water62%
In 1,4-dioxane; water
With sodium hydroxide In 1,4-dioxane
potassium tert-butylate
865-47-4

potassium tert-butylate

dimethyl 2-(10-methyl-9,10-dihydroacridin-9-yl)malonate
87442-43-1

dimethyl 2-(10-methyl-9,10-dihydroacridin-9-yl)malonate

A

10-methyl-9, 10-dihydro-9-acridinone
719-54-0

10-methyl-9, 10-dihydro-9-acridinone

B

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With oxygen In dimethyl sulfoxide at 70℃;A 50.4%
B n/a
dimethyl 2-(10-methyl-9,10-dihydroacridin-9-yl)malonate
87442-43-1

dimethyl 2-(10-methyl-9,10-dihydroacridin-9-yl)malonate

A

10-methyl-9, 10-dihydro-9-acridinone
719-54-0

10-methyl-9, 10-dihydro-9-acridinone

B

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With oxygen In dimethyl sulfoxide at 70℃;A 50.4%
B n/a
dimethyl 2-(10-methyl-9,10-dihydroacridin-9-yl)malonate
87442-43-1

dimethyl 2-(10-methyl-9,10-dihydroacridin-9-yl)malonate

A

10-methyl-9, 10-dihydro-9-acridinone
719-54-0

10-methyl-9, 10-dihydro-9-acridinone

B

tert-butyl formate
762-75-4

tert-butyl formate

C

carbon dioxide
124-38-9

carbon dioxide

Conditions
ConditionsYield
With potassium tert-butylate; oxygen In dimethyl sulfoxide at 60℃; Mechanism; other N-methyl-9-(dicarboalkoxymethyl)acridanes; chemiluminescent reaction;A 50.4%
B n/a
C n/a
(10-methyl-9,10-dihydro-acridin-9-yl)-malonic acid diethyl ester
87442-44-2

(10-methyl-9,10-dihydro-acridin-9-yl)-malonic acid diethyl ester

potassium tert-butylate
865-47-4

potassium tert-butylate

A

10-methyl-9, 10-dihydro-9-acridinone
719-54-0

10-methyl-9, 10-dihydro-9-acridinone

B

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With oxygen In dimethyl sulfoxide at 70℃;A 18%
B n/a
(10-methyl-9,10-dihydro-acridin-9-yl)-malonic acid diethyl ester
87442-44-2

(10-methyl-9,10-dihydro-acridin-9-yl)-malonic acid diethyl ester

A

10-methyl-9, 10-dihydro-9-acridinone
719-54-0

10-methyl-9, 10-dihydro-9-acridinone

B

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With oxygen In dimethyl sulfoxide at 70℃;A 18%
B n/a
tert-butyl methyl ether
1634-04-4

tert-butyl methyl ether

A

acetic acid methyl ester
79-20-9

acetic acid methyl ester

B

tert-butyl formate
762-75-4

tert-butyl formate

C

acetone
67-64-1

acetone

D

tert-butyl alcohol
75-65-0

tert-butyl alcohol

Conditions
ConditionsYield
With ozone In water at 20℃; pH=6.6 - 6.8; Kinetics; Oxidation; ultrasonic irradiation;A 3%
B 8%
C 12%
D 5%
With dihydrogen peroxide; iron(II) In water at 21.85℃; pH=3; Kinetics; Further Variations:; irradiation time; UV-irradiation;
potassium tert-butylate
865-47-4

potassium tert-butylate

2-(10-Methyl-9,10-dihydro-acridin-9-yl)-malonic acid diphenyl ester
87442-45-3

2-(10-Methyl-9,10-dihydro-acridin-9-yl)-malonic acid diphenyl ester

A

10-methyl-9, 10-dihydro-9-acridinone
719-54-0

10-methyl-9, 10-dihydro-9-acridinone

B

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With oxygen In dimethyl sulfoxide at 70℃;A 5.3%
B n/a
2-(10-Methyl-9,10-dihydro-acridin-9-yl)-malonic acid diphenyl ester
87442-45-3

2-(10-Methyl-9,10-dihydro-acridin-9-yl)-malonic acid diphenyl ester

A

10-methyl-9, 10-dihydro-9-acridinone
719-54-0

10-methyl-9, 10-dihydro-9-acridinone

B

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With oxygen In dimethyl sulfoxide at 70℃;A 5.3%
B n/a
formic acid
64-18-6

formic acid

tertiary butyl chloride
507-20-0

tertiary butyl chloride

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With calcium diformate
n-butyl formate
592-84-7

n-butyl formate

aluminum tri-tert-butoxide
556-91-2

aluminum tri-tert-butoxide

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
at 60℃; under 130 Torr;
formic acid
64-18-6

formic acid

isobutene
115-11-7

isobutene

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With sulfuric acid
With acidic cation exchanger
With sulfuric acid; tert-butyl alcohol at -20℃;
potassium tert-butylate
865-47-4

potassium tert-butylate

chloral
75-87-6

chloral

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With ethyl vinyl ether
di-tert-butoxy-methane
2568-93-6

di-tert-butoxy-methane

chloroform
67-66-3

chloroform

A

dichloromethane
75-09-2

dichloromethane

B

tertiary butyl chloride
507-20-0

tertiary butyl chloride

C

tert-butyl formate
762-75-4

tert-butyl formate

D

1,1,2,2-tetrachloroethane
79-34-5

1,1,2,2-tetrachloroethane

Conditions
ConditionsYield
With di-tert-butyl peroxide at 130℃; Rate constant; Mechanism;
di-tert-butoxy-methane
2568-93-6

di-tert-butoxy-methane

A

Isobutane
75-28-5

Isobutane

B

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With di-tert-butyl peroxide In chlorobenzene at 130 - 150℃; Rate constant; Mechanism; or without solvent;
Isobutane
75-28-5

Isobutane

formyloxy radical
16499-21-1

formyloxy radical

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
Thermodynamic data; Mechanism; calculated (BEBO and equibonding method) activation energies for hydrogen atom transfer reaction, anodic formylation;
Ethyl tert-butyl ether
637-92-3

Ethyl tert-butyl ether

A

formaldehyd
50-00-0

formaldehyd

B

acetic acid tert-butyl ester
540-88-5

acetic acid tert-butyl ester

C

methyl nitrate
598-58-3

methyl nitrate

D

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With nitrate radical In gas at -16.1 - 89.9℃; under 750.06 Torr; Mechanism; Kinetics;
Methyl formate
107-31-3

Methyl formate

potassium tert-butylate
865-47-4

potassium tert-butylate

tert-butyl formate
762-75-4

tert-butyl formate

Conditions
ConditionsYield
With oxygen In dimethyl sulfoxide at 70℃;
tert-butyl formate
762-75-4

tert-butyl formate

(2,6-bis[(di-tert-butylphosphino)methyl]phenyl)rhodium dinitrogen
219832-01-6

(2,6-bis[(di-tert-butylphosphino)methyl]phenyl)rhodium dinitrogen

(2,6-bis{(di-tert-butylphosphino)methyl}phenyl)carbonylrhodium(III)
60399-59-9

(2,6-bis{(di-tert-butylphosphino)methyl}phenyl)carbonylrhodium(III)

Conditions
ConditionsYield
In benzene-d6 byproducts: t-BuOH; N2, ligand (1.2-1.5 mmol) added to soln. of Rh compd. (1 mmol), stirred at room temp.; NMR;99%
tert-butyl formate
762-75-4

tert-butyl formate

tert-butyl N-[2-[(3-bromopyrazolo[1,5-a]pyrimidin-5-yl)amino]ethyl]-N-[2-[tert-butyl(dimethyl)silyl]oxyethyl]carbamate
1429313-20-1

tert-butyl N-[2-[(3-bromopyrazolo[1,5-a]pyrimidin-5-yl)amino]ethyl]-N-[2-[tert-butyl(dimethyl)silyl]oxyethyl]carbamate

tert-butyl N-(3-bromopyrazolo[1,5-a]pyrimidin-5-yl)-N-[2-[tert-butoxycarbonyl-[2-(tert-butyl(dimethyl)silyl)oxyethyl]amino]ethyl]carbamate
1429313-21-2

tert-butyl N-(3-bromopyrazolo[1,5-a]pyrimidin-5-yl)-N-[2-[tert-butoxycarbonyl-[2-(tert-butyl(dimethyl)silyl)oxyethyl]amino]ethyl]carbamate

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 70℃; for 4h;99%
(+/-)-1-[9-benzyl-3,9-diazabicyclo[4.2.1]non-9-yl]-propane-1-one

(+/-)-1-[9-benzyl-3,9-diazabicyclo[4.2.1]non-9-yl]-propane-1-one

tert-butyl formate
762-75-4

tert-butyl formate

(+/-)-9-benzyl-3,9-diazabicyclo[4.2.1]nonane-3-carboxylic acid tert-butyl ester
653600-90-9

(+/-)-9-benzyl-3,9-diazabicyclo[4.2.1]nonane-3-carboxylic acid tert-butyl ester

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran96%
tert-butyl formate
762-75-4

tert-butyl formate

C14H13BrN6O4S
1429313-59-6

C14H13BrN6O4S

C19H21BrN6O6S
1429323-70-5

C19H21BrN6O6S

Conditions
ConditionsYield
With dmap; triethylamine In tetrahydrofuran Reflux;96%
tert-butyl formate
762-75-4

tert-butyl formate

C13H17BrN4O2
1429323-62-5

C13H17BrN4O2

C18H25BrN4O4
1429323-63-6

C18H25BrN4O4

Conditions
ConditionsYield
With dmap; triethylamine In tetrahydrofuran Reflux;95%
tert-butyl formate
762-75-4

tert-butyl formate

5-chloro-2-methyl-benzenamine
95-79-4

5-chloro-2-methyl-benzenamine

tert-butyl (5-chloro-2-methylphenyl)carbamate
876353-89-8

tert-butyl (5-chloro-2-methylphenyl)carbamate

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; for 16h; Inert atmosphere;94%
tert-butyl formate
762-75-4

tert-butyl formate

Phenyl acetate
122-79-2

Phenyl acetate

phenyl (E)-3-(t-butoxy)acrylate

phenyl (E)-3-(t-butoxy)acrylate

Conditions
ConditionsYield
With titanium tetrachloride; triethylamine In dichloromethane at -20℃; for 1h; Inert atmosphere;94%
tert-butyl formate
762-75-4

tert-butyl formate

1,1,2,2,3,3-hexafluoro-1-[(1,2,2-trifluoroethenyl)oxy]-3-(trifluoromethoxy)-propane
40573-09-9

1,1,2,2,3,3-hexafluoro-1-[(1,2,2-trifluoroethenyl)oxy]-3-(trifluoromethoxy)-propane

tert-butyl 2,2,3-trifluoro-3-[1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propoxy]propanoate
1309689-72-2

tert-butyl 2,2,3-trifluoro-3-[1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propoxy]propanoate

Conditions
ConditionsYield
With at 52 - 55℃; for 24h; Product distribution / selectivity;93%
3-aminobutyric acid
2835-82-7

3-aminobutyric acid

tert-butyl formate
762-75-4

tert-butyl formate

3-t-butoxycarbonylaminobutyric acid
43080-09-7, 52815-19-7

3-t-butoxycarbonylaminobutyric acid

Conditions
ConditionsYield
With sodium hydroxide In 1,4-dioxane; water at 20℃;89.2%
tert-butyl formate
762-75-4

tert-butyl formate

Ti(N[t-Bu](3,5-Me2C6H3))3

Ti(N[t-Bu](3,5-Me2C6H3))3

titanium(IV)(N(tert-Bu)(3,5-Me2C6H3))3 formate
862887-61-4

titanium(IV)(N(tert-Bu)(3,5-Me2C6H3))3 formate

Conditions
ConditionsYield
In pentane at 24℃; for 0.5h; Inert atmosphere; Schlenk technique;88%
tert-butyl formate
762-75-4

tert-butyl formate

C20H24BrN5O2
1429323-90-9

C20H24BrN5O2

C25H32BrN5O4
1429323-91-0

C25H32BrN5O4

Conditions
ConditionsYield
With dmap; triethylamine In tetrahydrofuran Reflux;86%
tert-butyl formate
762-75-4

tert-butyl formate

2-oxabicyclo[3.2.1]octan-3-one
5724-61-8

2-oxabicyclo[3.2.1]octan-3-one

4-[1-Hydroxy-meth-(Z)-ylidene]-2-oxa-bicyclo[3.2.1]octan-3-one
59171-43-6

4-[1-Hydroxy-meth-(Z)-ylidene]-2-oxa-bicyclo[3.2.1]octan-3-one

Conditions
ConditionsYield
With potassium tert-butylate In tetrahydrofuran at 23℃; for 1.5h;85%
tert-butyl formate
762-75-4

tert-butyl formate

tert-butyl alcohol
75-65-0

tert-butyl alcohol

Conditions
ConditionsYield
dodecacarbonyl-triangulo-triruthenium; P(C4H9)3 In pyridine at 180℃; for 8h;84%
chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

tert-butyl formate
762-75-4

tert-butyl formate

diethyl 3-methylbut-2-enylphosphonate
51795-72-3

diethyl 3-methylbut-2-enylphosphonate

{1-[1-tert-Butoxy-meth-(Z)-ylidene]-3-methyl-but-2-enyl}-phosphonic acid diethyl ester

{1-[1-tert-Butoxy-meth-(Z)-ylidene]-3-methyl-but-2-enyl}-phosphonic acid diethyl ester

Conditions
ConditionsYield
With hydrogenchloride; lithium diisopropyl amide In tetrahydrofuran at -70℃; 2.) 10 min; 3.) pH=2;84%
tert-butyl formate
762-75-4

tert-butyl formate

1,1,2,3,3-pentafluoro-3-(1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propoxy)prop-1-ene
1193111-27-1

1,1,2,3,3-pentafluoro-3-(1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propoxy)prop-1-ene

tert-butyl 2,2,3,4,4-pentafluoro-4-[1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propoxy]butanoate
1309689-73-3

tert-butyl 2,2,3,4,4-pentafluoro-4-[1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propoxy]butanoate

Conditions
ConditionsYield
With at 55 - 58℃; for 32h;83%
tert-butyl formate
762-75-4

tert-butyl formate

C22H38O7
1431725-73-3

C22H38O7

C22H38O8

C22H38O8

Conditions
ConditionsYield
With bis(acetylacetonate)oxovanadium In benzene at 20℃; for 0.166667h;83%
tert-butyl formate
762-75-4

tert-butyl formate

tris(trimethylsilyl)silyllithium
4110-02-5

tris(trimethylsilyl)silyllithium

bis[tris(trimethylsilyl)silyl]methanol
192193-65-0

bis[tris(trimethylsilyl)silyl]methanol

Conditions
ConditionsYield
In pentane at -78℃;82%
tert-butyl formate
762-75-4

tert-butyl formate

Trimethylenediamine
109-76-2

Trimethylenediamine

N-Boc-1,3-diaminopropane
75178-96-0

N-Boc-1,3-diaminopropane

Conditions
ConditionsYield
In tetrahydrofuran at 0 - 20℃; for 24h;82%
tert-butyl formate
762-75-4

tert-butyl formate

TaH(η2-N(3,5-dimethylphenyl)CHtBu)(N(3,5-dimethylphenyl)CH2tBu)2

TaH(η2-N(3,5-dimethylphenyl)CHtBu)(N(3,5-dimethylphenyl)CH2tBu)2

Ta(OCH2OtBu)(η2-N(3,5-dimethylphenyl)CHtBu)(N(3,5-dimethylphenyl)CH2tBu)2

Ta(OCH2OtBu)(η2-N(3,5-dimethylphenyl)CHtBu)(N(3,5-dimethylphenyl)CH2tBu)2

Conditions
ConditionsYield
In not given treatment of tantalum compd. with formate deriv.;82%
tert-butyl formate
762-75-4

tert-butyl formate

C9H9BrN4O2
1429324-23-1

C9H9BrN4O2

C14H17BrN4O4
1429324-24-2

C14H17BrN4O4

Conditions
ConditionsYield
With dmap; triethylamine In tetrahydrofuran Reflux;82%
iodobenzene
591-50-4

iodobenzene

tert-butyl formate
762-75-4

tert-butyl formate

sodium methylate
124-41-4

sodium methylate

A

benzoic acid methyl ester
93-58-3

benzoic acid methyl ester

B

benzoic acid tert-butyl ester
774-65-2

benzoic acid tert-butyl ester

C

benzene
71-43-2

benzene

Conditions
ConditionsYield
bis-triphenylphosphine-palladium(II) chloride In dichloromethane at 40℃; under 750.06 Torr; for 1h;A 80%
B 11%
C 4%

762-75-4Relevant articles and documents

-

Closson,W.D.,Haug,P.

, p. 2384 - 2389 (1964)

-

Sonolytic destruction of methyl tert-butyl ether by ultrasonic irradiation: The role of O3, H2O2, frequency, and power density

Kang, Joon-Wun,Hung, Hui-Ming,Lin, Angela,Hoffmann, Michael R.

, p. 3199 - 3205 (1999)

The kinetics of degradation of methyl tert-butyl ether (MTBE) by ultrasonic irradiation in the presence of ozone as functions of applied frequencies and applied power are investigated. Experiments are performed over the frequency range of 205-1078 kHz. The higher overall reaction rates are observed at 358 and 618 kHz and then at 205 and 1078 kHz. The observed pseudo-first-order rate constant, k(O), for MTBE degradation increases with increasing power density up to 250 W L-1. A linear dependence of the first- order rate constant, k(O3), for the simultaneous degradation of O3 on power density is also observed. Naturally occurring organic matter (NOM) is shown to have a negligible effect on observed reaction rates. The kinetics of degradation of methyl tert-butyl ether (MTBE) by ultrasonic irradiation in the presence of ozone as functions of applied frequencies and applied power are investigated. Experiments are performed over the frequency range of 205-1078 kHz. The higher overall reaction rates are observed at 358 and 618 kHz and then at 205 and 1078 kHz. The observed pseudo-first-order rate constant, k0, for MTBE degradation increases with increasing power density up to 250 W L-1. A linear dependence of the first-order rate constant, kO(3), for the simultaneous degradation of O3 on power density is also observed. Naturally occurring organic matter (NOM) is shown to have a negligible effect on observed reaction rates.

PROCESS FOR MAKING FORMIC ACID UTILIZING LOWER-BOILING FORMATE ESTERS

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Paragraph 00177; 00178, (2019/02/15)

Disclosed is a process for recovering formic acid from a formate ester of a C3 to C4 alcohol. Disclosed is also a process for producing formic acid by carbonylating a C3 to C4 alcohol, hydrolyzing the formate ester of the alcohol, and recovering a formic acid product. The alcohol may be dried and returned to the reactor. The process enables a more energy efficient production of formic acid than the carbonylation of methanol to produce methyl formate.

Purified mCPBA, a Useful Reagent for the Oxidation of Aldehydes

Horn, Alexander,Kazmaier, Uli

, p. 2531 - 2536 (2018/03/21)

Purified mCPBA is a useful reagent for the oxidation of several classes of aldehyde. Although linear unbranched aliphatic aldehydes are oxidized to the corresponding carboxylic acids, α-branched ones undergo Baeyer–Villiger oxidation to formates. α-Branched α,β-unsaturated aldehydes provide enolformates and/or epoxides, which can be saponified to α-hydroxy ketones with shortening of the carbon chain by 1 carbon. Unbranched α,β-unsaturated aldehydes undergo an interesting Baeyer–Villiger oxidation/epoxidation/formate migration/BV oxidation cascade, which results in formyl-protected hydrates with an overall loss of two carbon atoms.

TiCl4/Et3N-Mediated Condensation of Acetate and Formate Esters: Direct Access to β-Alkoxy- and β-Aryloxyacrylates

álvarez-Calero, José María,Jorge, Zacarías D.,Massanet, Guillermo M.

supporting information, p. 6344 - 6347 (2016/12/23)

A methodology to build (E)-β-alkoxy- and (E)-β-aryloxyacrylate moieties from acetate and formate esters promoted by the TiCl4/Et3N system is presented. The reaction is compatible with a broad range of structural skeletons and elapses through an unusual condensation pathway. Taking into account the obtained results, we propose a plausible mechanism involving a bimetallic titanium intermediate for this type of transformation.

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