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1515-72-6 Usage

Chemical Properties

slight yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 1515-72-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1515-72:
(6*1)+(5*5)+(4*1)+(3*5)+(2*7)+(1*2)=66
66 % 10 = 6
So 1515-72-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO2/c1-2-3-8-13-11(14)9-6-4-5-7-10(9)12(13)15/h4-7H,2-3,8H2,1H3

1515-72-6 Well-known Company Product Price

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  • Alfa Aesar

  • (A16020)  N-(n-Butyl)phthalimide, 99%   

  • 1515-72-6

  • 5g

  • 417.0CNY

  • Detail
  • Alfa Aesar

  • (A16020)  N-(n-Butyl)phthalimide, 99%   

  • 1515-72-6

  • 25g

  • 1009.0CNY

  • Detail
  • Alfa Aesar

  • (A16020)  N-(n-Butyl)phthalimide, 99%   

  • 1515-72-6

  • 100g

  • 3382.0CNY

  • Detail
  • Aldrich

  • (730424)  N-Butylphthalimide  97%

  • 1515-72-6

  • 730424-25G

  • 604.89CNY

  • Detail
  • Aldrich

  • (730424)  N-Butylphthalimide  97%

  • 1515-72-6

  • 730424-100G

  • 1,572.48CNY

  • Detail

1515-72-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Butylphthalimide

1.2 Other means of identification

Product number -
Other names BUTYL PHTHALIMIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Finishing agents,Intermediates
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:1515-72-6 SDS

1515-72-6Synthetic route

phthalic anhydride
85-44-9

phthalic anhydride

N-butylamine
109-73-9

N-butylamine

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
for 0.0333333h; microwave irradiation;100%
In decaethylene glycol at 120℃; for 6h;98%
In water at 90 - 180℃; for 0.8h; Inert atmosphere;96.2%
carbon monoxide
201230-82-2

carbon monoxide

o-iodo-methyl-benzoic acid
610-97-9

o-iodo-methyl-benzoic acid

N-butylamine
109-73-9

N-butylamine

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 100℃; under 760.051 Torr; for 1h; Schlenk technique;100%
With triethylamine In toluene at 100℃;79%
1-bromo-butane
109-65-9

1-bromo-butane

phthalimide
136918-14-4

phthalimide

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With caesium carbonate In N,N-dimethyl-formamide at 70℃; for 0.166667h; Microwave irradiation;99%
With potassium carbonate In N,N-dimethyl-formamide at 40℃; for 18h; Inert atmosphere;98%
With potassium hydroxide; 1-butyl-3-methylimidazolium Tetrafluoroborate at 80℃; for 5h;94%
N-(3-butenyl)phthalimide
52898-32-5

N-(3-butenyl)phthalimide

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With Pd/C; C24H16N2O4 In ethanol at 50℃; for 18h; Glovebox;99%
1,2-Diiodobenzene
615-42-9

1,2-Diiodobenzene

carbon monoxide
201230-82-2

carbon monoxide

N-butylamine
109-73-9

N-butylamine

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With 1,4-diaza-bicyclo[2.2.2]octane; palladium 10% on activated carbon In toluene at 120℃; under 4654.46 Torr; for 2h; Autoclave;98%
With potassium carbonate In N,N-dimethyl-formamide at 100℃; under 760.051 Torr; for 4h; Schlenk technique;91%
carbon monoxide
201230-82-2

carbon monoxide

N-butylbenzamide
2782-40-3

N-butylbenzamide

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With potassium dihydrogenphosphate; Cp*Rh(MeCN)3[ClO4]2; silver carbonate In tert-Amyl alcohol at 100℃; under 760.051 Torr; for 24h;92%
2-Iodobenzoic acid
88-67-5

2-Iodobenzoic acid

carbon monoxide
201230-82-2

carbon monoxide

N-butylamine
109-73-9

N-butylamine

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With triethylamine In toluene at 100℃; for 4h;91%
1-bromo-butane
109-65-9

1-bromo-butane

potassium phtalimide
1074-82-4

potassium phtalimide

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
[2.2.2]cryptande In tetrahydrofuran for 0.166667h;90%
In N,N-dimethyl-formamide at 55℃;75%
1-iodo-butane
542-69-8

1-iodo-butane

potassium phtalimide
1074-82-4

potassium phtalimide

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 120℃; for 2h;90%
In N,N-dimethyl-formamide at 55℃;45%
n-Butyl chloride
109-69-3

n-Butyl chloride

potassium phtalimide
1074-82-4

potassium phtalimide

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
[2.2.2]cryptande In tetrahydrofuran for 0.666667h;90%
In N,N-dimethyl-formamide at 70℃; for 2h; Gabriel Amine Synthesis;28%
phthalimide
136918-14-4

phthalimide

N-butylamine
109-73-9

N-butylamine

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With dipotassium peroxodisulfate In water at 100℃; for 0.166667h; Microwave irradiation; Green chemistry;90%
With iron oxide In neat (no solvent) at 140℃; for 5h; Sealed tube;90%
With graphene oxide In neat (no solvent) at 130℃; for 12h; Sealed tube;88%
With citric acid-coated magnetic Fe3O4 nanoparticles In neat (no solvent) at 120℃; for 8h; Inert atmosphere;76%
With copper at 20 - 40℃; for 3h;70%
phthalimide
136918-14-4

phthalimide

n-Butyl chloride
109-69-3

n-Butyl chloride

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With potassium fluoride; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate at 85℃; for 8h;88%
phthalic anhydride
85-44-9

phthalic anhydride

N-[(butylamino)carbonyl]-4-methyl-benzenesulfonamide
64-77-7

N-[(butylamino)carbonyl]-4-methyl-benzenesulfonamide

A

N-butylphthalimide
1515-72-6

N-butylphthalimide

B

toluene-4-sulfonamide
70-55-3

toluene-4-sulfonamide

Conditions
ConditionsYield
With pyridine; dmap for 4h; Heating;A 86%
B 50%
N-[(butylamino)carbonyl]-4-methyl-benzenesulfonamide
64-77-7

N-[(butylamino)carbonyl]-4-methyl-benzenesulfonamide

A

N-butylphthalimide
1515-72-6

N-butylphthalimide

B

toluene-4-sulfonamide
70-55-3

toluene-4-sulfonamide

Conditions
ConditionsYield
With pyridine; dmap; phthalic anhydride for 4h; Heating;A 86%
B 50%
N-butylamine
109-73-9

N-butylamine

molybdenum hexacarbonyl
13939-06-5, 199620-15-0

molybdenum hexacarbonyl

1,2-dibromobenzene
583-53-9

1,2-dibromobenzene

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With palladium diacetate; 1,8-diazabicyclo[5.4.0]undec-7-ene; catacxium A In toluene at 100℃; for 16h; Reagent/catalyst; Sealed tube; Inert atmosphere;84%
o-iodo-methyl-benzoic acid
610-97-9

o-iodo-methyl-benzoic acid

n-butyl isocyanide
111-36-4

n-butyl isocyanide

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With triethylamine; 1,2-bis-(diphenylphosphino)ethane; zinc; dibromo[1,2-bis(diphenylphosphino)ethane]nickel(II) In acetonitrile at 80℃; for 36h;82%
N-methoxyphthalimide
1914-20-1

N-methoxyphthalimide

N-butylamine
109-73-9

N-butylamine

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
In ethanol for 4h;81%
phthalic anhydride
85-44-9

phthalic anhydride

carbutamide
339-43-5

carbutamide

A

N-butylphthalimide
1515-72-6

N-butylphthalimide

B

4-(1,3-dioxobenzo[c]azolidin-2-yl)benzenesulfonamide
4479-70-3

4-(1,3-dioxobenzo[c]azolidin-2-yl)benzenesulfonamide

C

4-Phthalylaminobenzolsulfonamid

4-Phthalylaminobenzolsulfonamid

Conditions
ConditionsYield
With pyridine; dmap for 4h; Heating;A 45%
B 76%
C 7%
N-hydroxyphthalimide
524-38-9

N-hydroxyphthalimide

N-butylamine
109-73-9

N-butylamine

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
In ethanol for 4h;76%
potassium phtalimide
1074-82-4

potassium phtalimide

butan-1-ol
71-36-3

butan-1-ol

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With 1,3,5-trichloro-2,4,6-triazine; N,N-dimethyl-formamide In dichloromethane at 25 - 65℃;76%
With 1,3,5-trichloro-2,4,6-triazine; C2F6NO4S2(1-)*C8H14N3O(1+) In acetonitrile at 65℃; for 4h;82 %Chromat.
phthalimide
136918-14-4

phthalimide

butan-1-ol
71-36-3

butan-1-ol

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With di-isopropyl azodicarboxylate; (1,3,4)-triphenyl-4,5-dihydro-1H-1,2,4-triazol-5-ylidene In 1,4-dioxane; toluene at 80℃; for 12h; Inert atmosphere;76%
With DMAM; triphenylphosphine In tetrahydrofuran at 20℃; Mitsunobu Displacement;62%
carbon monoxide
201230-82-2

carbon monoxide

benzaldehyde
100-52-7

benzaldehyde

N-butylamine
109-73-9

N-butylamine

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
Stage #1: benzaldehyde; N-butylamine With dichloro bis(acetonitrile) palladium(II); copper(II) oxide In N,N-dimethyl-formamide; toluene at 20℃; for 12h;
Stage #2: carbon monoxide With oxygen In N,N-dimethyl-formamide; toluene at 100℃;
75%
Stage #1: benzaldehyde; N-butylamine With dichloro bis(acetonitrile) palladium(II); copper(II) oxide In N,N-dimethyl-formamide; toluene at 20℃; for 12h; Green chemistry;
Stage #2: carbon monoxide With oxygen In N,N-dimethyl-formamide; toluene at 100℃; under 760.051 Torr; for 48h; Green chemistry;
75%
carbon monoxide
201230-82-2

carbon monoxide

(E)-N-benzylidenebutan-1-amine
57527-55-6

(E)-N-benzylidenebutan-1-amine

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With dichloro bis(acetonitrile) palladium(II); water; oxygen; copper(II) oxide In N,N-dimethyl-formamide; toluene at 100℃; for 24h; Temperature;75%
N-butylisophthalimide
80991-83-9

N-butylisophthalimide

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
at 200℃; for 0.25h;70%
2-n-butylisoindoline
20138-24-3

2-n-butylisoindoline

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With tert.-butylhydroperoxide; copper(l) chloride In dichloromethane; water at 50℃; for 24h; Reagent/catalyst; Solvent; Temperature; Sealed tube;68%
phthalimide
136918-14-4

phthalimide

N,N'-Dicyclohexyl-O-butyl-isoharnstoff
6738-16-5

N,N'-Dicyclohexyl-O-butyl-isoharnstoff

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 120℃; for 2h;66%
n-butyl isonitrile
2769-64-4

n-butyl isonitrile

carbon dioxide
124-38-9

carbon dioxide

2-(trimethylsilyl)phenyl trifluoromethanesulfonate
88284-48-4

2-(trimethylsilyl)phenyl trifluoromethanesulfonate

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With cesium fluoride In acetonitrile at 30℃; for 24h; Inert atmosphere;64%
2-(4-bromobutyl)isoindoline-1,3-dione
5394-18-3

2-(4-bromobutyl)isoindoline-1,3-dione

(-)-norcocaine
18717-72-1

(-)-norcocaine

N-butylphthalimide
1515-72-6

N-butylphthalimide

Conditions
ConditionsYield
With sodium carbonate In benzene60%
N-butylphthalimide
1515-72-6

N-butylphthalimide

vinyl magnesium bromide
1826-67-1

vinyl magnesium bromide

2-butyl-3-hydroxy-3-vinylisoindolin-1-one

2-butyl-3-hydroxy-3-vinylisoindolin-1-one

Conditions
ConditionsYield
In tetrahydrofuran; hexane at -30 - -5℃;95%
N-butylphthalimide
1515-72-6

N-butylphthalimide

4-nitro-N-butylphthalimide
54395-37-8

4-nitro-N-butylphthalimide

Conditions
ConditionsYield
With sulfuric acid; nitric acid at 80℃; for 0.0666667h; Temperature;95%
N-butylphthalimide
1515-72-6

N-butylphthalimide

2-butyl-3-hydroxyisoindolin-1-one
100390-46-3

2-butyl-3-hydroxyisoindolin-1-one

Conditions
ConditionsYield
With ethanol; tetrabutylammonium tetrafluoroborate; diisopropylamine at 20℃; for 2h; Electrochemical reaction; Schlenk technique; Green chemistry; chemoselective reaction;93%
With titanium tetrachloride; potassium carbonate; zinc 1.) 110 deg C, 20 h; Yield given. Multistep reaction;
N-butylphthalimide
1515-72-6

N-butylphthalimide

2-butyl-2,3-dihydro-isoindol-1-one
50707-36-3

2-butyl-2,3-dihydro-isoindol-1-one

Conditions
ConditionsYield
With ethanol; tetrabutylammonium tetrafluoroborate; diisopropylamine at 20℃; for 2.75h; Electrochemical reaction; Schlenk technique; Green chemistry; chemoselective reaction;92%
With tetrabutyl ammonium fluoride In tetrahydrofuran at 25℃; Inert atmosphere;72%
With hydrogenchloride; mercury; zinc In water at 100℃; for 5h;32%
N-butylphthalimide
1515-72-6

N-butylphthalimide

nitro-N-butylphthalimide

nitro-N-butylphthalimide

Conditions
ConditionsYield
With nitric acid In sulfuric acid90%
With nitric acid0.1% by weight
N-butylphthalimide
1515-72-6

N-butylphthalimide

Methoxyallene
13169-00-1

Methoxyallene

2-butyl-3-hydroxy-3-(1-methoxy-propa-1,2-dienyl)-2,3-dihydro-isoindol-1-one
403741-24-2

2-butyl-3-hydroxy-3-(1-methoxy-propa-1,2-dienyl)-2,3-dihydro-isoindol-1-one

Conditions
ConditionsYield
Stage #1: Methoxyallene With n-butyllithium In tetrahydrofuran; hexane
Stage #2: N-butylphthalimide In tetrahydrofuran; hexane at -78℃;
89%
methanol
67-56-1

methanol

N-butylphthalimide
1515-72-6

N-butylphthalimide

2-butyl-2,3-dihydro-3-methoxy-1H-isoindol-1-one

2-butyl-2,3-dihydro-3-methoxy-1H-isoindol-1-one

Conditions
ConditionsYield
With cobalt(II) tetrafluoroborate hexahydrate; hydrogen; [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] at 90℃; under 15001.5 Torr; for 18h; Sealed tube; Autoclave; Green chemistry;89%
With tris(2,4-pentanedionato)ruthenium(III); methanesulfonic acid; hydrogen; [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] at 130℃; under 11251.1 Torr; for 18h; Autoclave;88%
N-butylphthalimide
1515-72-6

N-butylphthalimide

N-butylbenzamide
2782-40-3

N-butylbenzamide

Conditions
ConditionsYield
With 1-methyl-pyrrolidin-2-one; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; water; potassium carbonate at 150℃; for 24h; Schlenk technique; Inert atmosphere; chemoselective reaction;88%
N-butylphthalimide
1515-72-6

N-butylphthalimide

7-bromo-hept-1-ene
4117-09-3

7-bromo-hept-1-ene

C19H27NO2

C19H27NO2

Conditions
ConditionsYield
Stage #1: 7-bromo-hept-1-ene With magnesium In tetrahydrofuran at 25℃; for 1h; Inert atmosphere;
Stage #2: N-butylphthalimide In tetrahydrofuran at 0℃; for 0.25h; Inert atmosphere;
83%
N-butylphthalimide
1515-72-6

N-butylphthalimide

cyclohexylamine
108-91-8

cyclohexylamine

N-Butyl-N'-cyclohexyl-phthalamide
103606-47-9

N-Butyl-N'-cyclohexyl-phthalamide

Conditions
ConditionsYield
In benzene at 20℃; for 72h;78%

1515-72-6Relevant articles and documents

N-Alkylphthalimides: Structural requirement of thalidomidal action on 12-O-tetradecanoylphorbol-13-acetate-induced tumor necrosis factor α production by human leukemia HL-60 cells

Shibata,Shichita,Sasaki,Nishimura,Hashimoto,Iwasaki

, p. 177 - 179 (1995)

Phthalimide analogs N-substituted with n-butyl, tert-butyl, hexyl and adamantyl groups were designed and prepared as simplified analogs of thalidomide and methylthalidomide. All the compounds prepared except N-n-butylphthalimide showed thalidomidal activity on 12-O-tetradecanoylphorbol-13-acetate-induced tumor necrosis factor (TNF)-α production by human leukemia HL-60 cells. Among the investigated compounds, including thalidomide and methylthalidomide, N-adamantylphthalimide showed the most potent TNF-α production-enhancing activity.

Copper-catalyzed oxidation of arene-fused cyclic amines to cyclic imides

Yan, Xiaoyu,Fang, Kun,Liu, Hailan,Xi, Chanjuan

, p. 10650 - 10652 (2013)

A novel copper-catalyzed oxidation of arene-fused cyclic amines to the corresponding cyclic imides has been developed. The reaction can be used to synthesize 1,3-disubstituted TPD in high yields.

Carbonylative cyclization of o-halobenzoic acids for synthesis of N-substituted phthalimides using polymer-supported palladium-N-heterocyclic carbene as an efficient, heterogeneous, and reusable catalyst

Khedkar, Mayur V.,Khan, Shoeb R.,Dhake, Kishor P.,Bhanage, Bhalchandra M.

, p. 2623 - 2629 (2012)

The carbonylative cyclization of o-iodobenzoic acid with a variety of primary amines and carbon monoxide (1 bar) using a polymer-supported palladium-N-heterocyclic carbene complex (PS-Pd-NHC) as the catalyst gives N-substituted 1H-isoindole-1,3(2H)-diones (phthalimides) in good to excellent yields with a short reaction time. The catalyst is efficient, heterogeneous, and phosphine-free, it exhibited remarkable activity and it is also recyclable (4 consecutive cycles). The use of methyl o-iodobenzoate as the substrate under these conditions also gave N-substituted 1H-isoindole-1,3(2H)-diones, but with lower yields. Cyclization of o-iodobenzyl alcohol with carbon monoxide under these conditions gave isobenzofuran-1(3H)-one (phthalide). Georg Thieme Verlag Stuttgart · New York.

Electroselective and Controlled Reduction of Cyclic Imides to Hydroxylactams and Lactams

Bai, Ya,Shi, Lingling,Zheng, Lianyou,Ning, Shulin,Che, Xin,Zhang, Zhuoqi,Xiang, Jinbao

supporting information, p. 2298 - 2302 (2021/04/05)

An efficient and practical electrochemical method for selective reduction of cyclic imides has been developed using a simple undivided cell with carbon electrodes at room temperature. The reaction provides a useful strategy for the rapid synthesis of hydroxylactams and lactams in a controllable manner, which is tuned by electric current and reaction time, and exhibits broad substrate scope and high functional group tolerance even to reduction-sensitive moieties. Initial mechanistic studies suggest that the approach heavily relies on the utilization of amines (e.g., i-Pr2NH), which are able to generate α-aminoalkyl radicals. This protocol provides an efficient route for the cleavage of C-O bonds under mild conditions with high chemoselectivity.

Preparation method of N - alkyl -4 -nitrophthalimide

-

Paragraph 0049-0050, (2021/10/27)

The invention discloses a preparation method of N - alkyl -4 -nitrophthalimide, which comprises the following steps of 1) mixing phthalic anhydride, alkyl aldehyde and inorganic amine, reacting under the action of hydrogen, cooling and crystallizing, and drying to obtain N -alkyl phthalimide. Step 2) The 1 alkylphthalimide obtained in step N -) is subjected to nitration reaction, and the product is purified and dried to obtain the N -alkyl -4 -nitrophthalimide. The alkyl aldehyde in step 1) is preferably an alkyl aldehyde of carbon 1 - 4. The preparation method has the advantages of wide raw material source, low price, simple process, easiness in large-scale production and the like. Through one-step synthesis, the reaction efficiency is high, the device is simple and easy to operate, and green and environment-friendly.

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