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623-68-7

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623-68-7 Usage

Chemical Properties

Colorless to pale yellow liquid

Synthesis Reference(s)

Tetrahedron Letters, 33, p. 593, 1992 DOI: 10.1016/S0040-4039(00)92318-9

Check Digit Verification of cas no

The CAS Registry Mumber 623-68-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 623-68:
(5*6)+(4*2)+(3*3)+(2*6)+(1*8)=67
67 % 10 = 7
So 623-68-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H10O3/c1-3-5-7(9)11-8(10)6-4-2/h3-6H,1-2H3/b5-3+,6-4+

623-68-7SDS

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 Crotonic Anhydride

1.2 Other means of identification

Product number -
Other names Crotonic anhydride

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:623-68-7 SDS

623-68-7Synthetic route

(E)-but-2-enoic acid
107-93-7

(E)-but-2-enoic acid

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

Conditions
ConditionsYield
With 2-chloro-1,3-dimethylimidazolinium chloride; triethylamine In dichloromethane at 20℃; for 18h; Acylation;96%
With dicyclohexyl-carbodiimide
4-methyleneoxetan-2-one
674-82-8

4-methyleneoxetan-2-one

2-butenoic acid
3724-65-0

2-butenoic acid

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

Conditions
ConditionsYield
With 1,4-dioxane at 70 - 80℃; folgendes Destillieren des Reaktionsgemisches;
2-butenoic acid
3724-65-0

2-butenoic acid

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

Conditions
ConditionsYield
With acetic anhydride
(E)-but-2-enoic acid
107-93-7

(E)-but-2-enoic acid

ethynyl methyl ether
6443-91-0

ethynyl methyl ether

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

Conditions
ConditionsYield
With dichloromethane; mercury(II) oxide
crotonyl chloride
10487-71-5

crotonyl chloride

triethylamine
121-44-8

triethylamine

benzene
71-43-2

benzene

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

diethyl ether
60-29-7

diethyl ether

(E)-but-2-enoic acid
107-93-7

(E)-but-2-enoic acid

1-ethoxyacetylene
927-80-0

1-ethoxyacetylene

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

(E)-but-2-enoic acid
107-93-7

(E)-but-2-enoic acid

1-ethoxyacetylene
927-80-0

1-ethoxyacetylene

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

Conditions
ConditionsYield
With diethyl ether
crotonaldehyde
123-73-9

crotonaldehyde

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

Conditions
ConditionsYield
With oxygen; cobalt(II) acetate; acetic acid at 30℃; unter leichtem Ueberdruck;
With oxygen; copper (I) acetate; acetic acid at 30℃; unter leichtem Ueberdruck;
With oxygen; manganese(II) acetate; acetic acid at 30℃; unter leichtem Ueberdruck;
With oxygen; acetic acid at 30℃; in Gegenwart einer Mischung von Wismut-,Kobalt- und Kupferpulver;
trans-chrotonyl chloride
625-35-4, 3488-22-0, 10487-71-5

trans-chrotonyl chloride

crotonate of sodium

crotonate of sodium

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

sodium crotonate

sodium crotonate

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

Conditions
ConditionsYield
With thionyl chloride; Petroleum ether
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

methyl 2-O-benzyl-4,6-di-O-methyl-α-D-mannopyranoside
366801-82-3

methyl 2-O-benzyl-4,6-di-O-methyl-α-D-mannopyranoside

methyl 2-O-benzyl-3-O-crotonyl-4,6-di-O-methyl-α-D-mannopyranoside
366801-85-6

methyl 2-O-benzyl-3-O-crotonyl-4,6-di-O-methyl-α-D-mannopyranoside

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 16h;100%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

polymer, product of radical polymerization, loading of chiral auxiliary 2.42 mmol/g, Mn=5800, Mw=7000 (GPC, polystyrene standards); monomer(S): styrene; (4S)-4-{4-[(4-vinylbenzyl)oxy]benzyl}-1,3-oxazolidin-2-one

polymer, product of radical polymerization, loading of chiral auxiliary 2.42 mmol/g, Mn=5800, Mw=7000 (GPC, polystyrene standards); monomer(S): styrene; (4S)-4-{4-[(4-vinylbenzyl)oxy]benzyl}-1,3-oxazolidin-2-one

polymer, loading of chiral auxiliary 2.42 mmol/g, Mn=7500, Mw=10000 (GPC, polystyrene standards); monomer(s): styrene; (4S)-4-{4-[(4-vinylbenzyl)oxy]benzyl}-1,3-oxazolidin-2-one; trans-crotonic anhydride

polymer, loading of chiral auxiliary 2.42 mmol/g, Mn=7500, Mw=10000 (GPC, polystyrene standards); monomer(s): styrene; (4S)-4-{4-[(4-vinylbenzyl)oxy]benzyl}-1,3-oxazolidin-2-one; trans-crotonic anhydride

Conditions
ConditionsYield
With dmap; triethylamine In tetrahydrofuran at 70℃; for 48h;100%
methyl 6-deoxy-2,3-bis-O-(phenylmethyl)-α-D-glucopyranoside
56750-58-4

methyl 6-deoxy-2,3-bis-O-(phenylmethyl)-α-D-glucopyranoside

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

methyl 2,3-di-O-benzyl-4-O-crotonyl-6-deoxy-α-D-glucopyranoside
250687-53-7

methyl 2,3-di-O-benzyl-4-O-crotonyl-6-deoxy-α-D-glucopyranoside

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 20.5h;99%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

methyl 2,4,6-tri-O-benzyl-α-D-galactopyranoside
55697-50-2

methyl 2,4,6-tri-O-benzyl-α-D-galactopyranoside

methyl 2,4,6-tri-O-benzyl-3-O-crotonyl-α-D-galactopyranoside

methyl 2,4,6-tri-O-benzyl-3-O-crotonyl-α-D-galactopyranoside

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 120h;98%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

methyl-2,3-di-O-benzyl-6-O-(4-toluenesulfonyl)-α-D-glucopyranoside
54522-57-5

methyl-2,3-di-O-benzyl-6-O-(4-toluenesulfonyl)-α-D-glucopyranoside

methyl 2,3-di-O-benzyl-4-O-crotonyl-6-O-p-toluenesulfonyl-α-D-glucopyranoside
366801-70-9

methyl 2,3-di-O-benzyl-4-O-crotonyl-6-O-p-toluenesulfonyl-α-D-glucopyranoside

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 23h;98%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

methyl 2,3-di-O-pivaloyl-6-O-p-toluenesulfonyl-α-D-glucopyranoside
366801-67-4

methyl 2,3-di-O-pivaloyl-6-O-p-toluenesulfonyl-α-D-glucopyranoside

methyl 4-O-crotonyl-2,3-di-O-pivaloyl-6-O-p-toluenesulfonyl-α-D-glucopyranoside
366801-69-6

methyl 4-O-crotonyl-2,3-di-O-pivaloyl-6-O-p-toluenesulfonyl-α-D-glucopyranoside

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 23h;98%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

(S)-4-Benzyl-2-oxazolidinone
90719-32-7

(S)-4-Benzyl-2-oxazolidinone

(4S)-3-((E)-2-butenoyl)-4-benzyl-2-oxazolidinone
90719-30-5

(4S)-3-((E)-2-butenoyl)-4-benzyl-2-oxazolidinone

Conditions
ConditionsYield
With triethylamine; lithium chloride In tetrahydrofuran at -15 - 20℃; for 12h;97%
With triethylamine; lithium chloride In tetrahydrofuran for 4h; Ambient temperature;88%
methyl O-2,3,6-tri-O-benzyl-α-D-glucopyranoside
19488-48-3

methyl O-2,3,6-tri-O-benzyl-α-D-glucopyranoside

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

methyl 2,3,6-tri-O-benzyl-4-O-crotonyl-α-D-glucopyranoside

methyl 2,3,6-tri-O-benzyl-4-O-crotonyl-α-D-glucopyranoside

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 21h;97%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

(1S,2R)-1,2-diphenylethane-1,2-diol
579-43-1

(1S,2R)-1,2-diphenylethane-1,2-diol

meso-hydrobenzoin mono-trans-crotonate

meso-hydrobenzoin mono-trans-crotonate

Conditions
ConditionsYield
With ytterbium(III) chloride In tetrahydrofuran97%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

5-(2-((4S,6R)-6-((2S,3S)-3-(benzyloxy)-2-hydroxybutyl)-2,2-diisopropyl-1,3,2-dioxasilinan-4-yl)propan-2-yl)furan-2-carbaldehyde
1352481-42-5

5-(2-((4S,6R)-6-((2S,3S)-3-(benzyloxy)-2-hydroxybutyl)-2,2-diisopropyl-1,3,2-dioxasilinan-4-yl)propan-2-yl)furan-2-carbaldehyde

(E)-((2S,3S)-3-(benzyloxy)-1-((4R,6S)-6-(2-(5-formylfuran-2-yl)propan-2-yl)-2,2-diisopropyl-1,3,2-dioxasilinan-4-yl)butan-2-yl) but-2-enoate
1352481-43-6

(E)-((2S,3S)-3-(benzyloxy)-1-((4R,6S)-6-(2-(5-formylfuran-2-yl)propan-2-yl)-2,2-diisopropyl-1,3,2-dioxasilinan-4-yl)butan-2-yl) but-2-enoate

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane at 0℃; for 4h; Inert atmosphere;97%
2-[2-((tert-butyldimethylsilanyloxy)methyl)phenyl]propan-1-ol
942062-83-1

2-[2-((tert-butyldimethylsilanyloxy)methyl)phenyl]propan-1-ol

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

but-2-enoic acid 2-[2-((tert-butyldimethylsilanyloxy)methyl)phenyl]propyl ester
942062-84-2

but-2-enoic acid 2-[2-((tert-butyldimethylsilanyloxy)methyl)phenyl]propyl ester

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane at 0℃; for 4h;96%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

1-adamanthanol
768-95-6

1-adamanthanol

1-Adamantyl crotonate
134690-47-4

1-Adamantyl crotonate

Conditions
ConditionsYield
Acidic catalyst In cyclohexane Heating;95%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

1,3-dimethyl-5-adamantanol
707-37-9

1,3-dimethyl-5-adamantanol

3,5-Dimethyl-1-adamantyl crotonate
134690-48-5

3,5-Dimethyl-1-adamantyl crotonate

Conditions
ConditionsYield
Acidic catalyst In cyclohexane Heating;95%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

(1R,2R,3S,4R)-3-O-tert-Butyldimethylsilyl-1,2-O-cyclohexylidene-5-hydroxymethyl-5-cyclohexen-1,2,3,4-tetraol
128044-91-7

(1R,2R,3S,4R)-3-O-tert-Butyldimethylsilyl-1,2-O-cyclohexylidene-5-hydroxymethyl-5-cyclohexen-1,2,3,4-tetraol

(1R,2R,3S,4R)-3-O-tert-Butyldimethylsilyl-5-crotonyloxymethyl-1,2-O-cyclohexylidene-5-cyclohexen-1,2,3,4-tetraol
128044-92-8

(1R,2R,3S,4R)-3-O-tert-Butyldimethylsilyl-5-crotonyloxymethyl-1,2-O-cyclohexylidene-5-cyclohexen-1,2,3,4-tetraol

Conditions
ConditionsYield
With pyridine; dmap In dichloromethane95%
With pyridine; dmap In dichloromethane for 12h; Ambient temperature;95%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

methyl 6-deoxy-2,3-di-O-methyl-α-D-glucopyranoside
62853-52-5

methyl 6-deoxy-2,3-di-O-methyl-α-D-glucopyranoside

methyl 4-O-crotonyl-6-deoxy-2,3-di-O-methyl-α-D-glucopyranoside
250687-55-9

methyl 4-O-crotonyl-6-deoxy-2,3-di-O-methyl-α-D-glucopyranoside

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 13h;95%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

(S)-4-benzyl-5,5-dimethyloxazolidin-2-one
168297-85-6

(S)-4-benzyl-5,5-dimethyloxazolidin-2-one

(S)-3-((E)-but-2-enoyl)-4-benzyl-5,5-dimethyloxazolidin-2-one
618436-90-1

(S)-3-((E)-but-2-enoyl)-4-benzyl-5,5-dimethyloxazolidin-2-one

Conditions
ConditionsYield
With triethylamine; lithium chloride In tetrahydrofuran at -78 - 20℃; for 12h;94%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

6-(piperazin-1-yl)pyridine-3-carbonitrile dihydrochloride

6-(piperazin-1-yl)pyridine-3-carbonitrile dihydrochloride

6-[4-[(2E)-but-2-enoyl]piperazin-1-yl]pyridine-3-carbonitrile

6-[4-[(2E)-but-2-enoyl]piperazin-1-yl]pyridine-3-carbonitrile

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20 - 30℃; for 1h;94%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

methyl 6-deoxy-2,3-di-O-pivaloyl-α-D-glucopyranoside
366801-72-1

methyl 6-deoxy-2,3-di-O-pivaloyl-α-D-glucopyranoside

methyl 4-O-crotonyl-6-deoxy-2,3-di-O-pivaloyl-α-D-glucopyranoside
250687-54-8

methyl 4-O-crotonyl-6-deoxy-2,3-di-O-pivaloyl-α-D-glucopyranoside

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 19h;93%
methyl 2,3,4-tri-O-benzyl-D-glucopyranoside
53008-65-4

methyl 2,3,4-tri-O-benzyl-D-glucopyranoside

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

methyl 2,3,4-tri-O-benzyl-6-O-crotonyl-α-D-glucopyranoside

methyl 2,3,4-tri-O-benzyl-6-O-crotonyl-α-D-glucopyranoside

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 18h;92%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

methyl 2,3-di-O-benzyl-6-O-pivaloyl-α-D-glucopyranoside
184715-41-1

methyl 2,3-di-O-benzyl-6-O-pivaloyl-α-D-glucopyranoside

methyl 2,3-di-O-benzyl-4-O-crotonyl-6-O-pivaloyl-α-D-glucopyranoside
250687-57-1

methyl 2,3-di-O-benzyl-4-O-crotonyl-6-O-pivaloyl-α-D-glucopyranoside

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 7h;92%
dimethylenecyclourethane
497-25-6

dimethylenecyclourethane

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

3-((E)-but-2-enoyl)oxazolidin-2-one
109299-92-5

3-((E)-but-2-enoyl)oxazolidin-2-one

Conditions
ConditionsYield
With triethylamine; lithium chloride In tetrahydrofuran92%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

10-trans crotonyl-10-desacetylbaccatin III

10-trans crotonyl-10-desacetylbaccatin III

Conditions
ConditionsYield
With cerium(III) chloride In tetrahydrofuran at 25℃; for 20h; Under N2;91%
cerium(III) chloride In tetrahydrofuran at 25℃; for 20h;91%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

(E)-N-(4-(3-hydroxyhexa-1,5-dien-1-yl)phenyl)nicotinamide

(E)-N-(4-(3-hydroxyhexa-1,5-dien-1-yl)phenyl)nicotinamide

(E)-1-(4-(nicotinamido)phenyl)hexa-1,5-dien-3-yl (E)-but-2-enoate

(E)-1-(4-(nicotinamido)phenyl)hexa-1,5-dien-3-yl (E)-but-2-enoate

Conditions
ConditionsYield
Stage #1: (E)-N-(4-(3-hydroxyhexa-1,5-dien-1-yl)phenyl)nicotinamide With dmap; triethylamine In dichloromethane at 0℃;
Stage #2: trans-crotonic anhydride In dichloromethane at 0 - 20℃; for 3h;
90%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

trimethylsilyl cyanide
7677-24-9

trimethylsilyl cyanide

benzaldehyde
100-52-7

benzaldehyde

(E)-But-2-enoic acid cyano-phenyl-methyl ester

(E)-But-2-enoic acid cyano-phenyl-methyl ester

Conditions
ConditionsYield
Stage #1: trimethylsilyl cyanide; benzaldehyde; iron(III) chloride In nitromethane at 0℃; for 0.5h;
Stage #2: trans-crotonic anhydride In nitromethane at 20℃; for 3h;
89%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

carbon monoxide
201230-82-2

carbon monoxide

2-bromoaniline
615-36-1

2-bromoaniline

(E)-2-(prop-1-en-1-yl)-4H-benzo[d][1,3]oxazin-4-one
1217821-56-1

(E)-2-(prop-1-en-1-yl)-4H-benzo[d][1,3]oxazin-4-one

Conditions
ConditionsYield
With potassium tetrachloropalladate(II); N-ethyl-N,N-diisopropylamine; catacxium A In toluene at 100℃; under 1500.15 Torr; for 16h; Autoclave;88%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

ethyl 3-((4R,5R)-5-((3S,4R,E)-4-((tert-butyldimethylsilyl)oxy)-3-hydroxypent- 1-en-1-yl)-2,2-dimethyl-1,3-dioxolan-4-yl)propanoate

ethyl 3-((4R,5R)-5-((3S,4R,E)-4-((tert-butyldimethylsilyl)oxy)-3-hydroxypent- 1-en-1-yl)-2,2-dimethyl-1,3-dioxolan-4-yl)propanoate

(3S,4R,E)-4-((tert-butyldimethylsilyl)oxy)-1-((4R,5R)-5-(3-ethoxy-3-oxopropyl)- 2,2-dimethyl-1,3-dioxolan-4-yl)pent-1-en-3-yl (E)-but-2-enoate

(3S,4R,E)-4-((tert-butyldimethylsilyl)oxy)-1-((4R,5R)-5-(3-ethoxy-3-oxopropyl)- 2,2-dimethyl-1,3-dioxolan-4-yl)pent-1-en-3-yl (E)-but-2-enoate

Conditions
ConditionsYield
With dmap In pyridine at 20℃; for 5h;88%
trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

(2R)-bornane-10,2-sultam
94594-90-8

(2R)-bornane-10,2-sultam

(1S)-N-crotyl-2,10-camphorsultam
94668-55-0

(1S)-N-crotyl-2,10-camphorsultam

Conditions
ConditionsYield
With triethylamine; lithium chloride In tetrahydrofuran for 4h; Ambient temperature;87%
(4S,5R)-4-benzyl-5-(1'H,1'H,2'H,2'H-perfluorooctyl)-oxazolidin-2-one
857637-92-4

(4S,5R)-4-benzyl-5-(1'H,1'H,2'H,2'H-perfluorooctyl)-oxazolidin-2-one

trans-crotonic anhydride
623-68-7

trans-crotonic anhydride

(E)-(4S,5R)-4-benzyl-3-(2'-butenoyl)-5-(1'H,1'H,2'H,2'H-perfluorooctyl)-2-oxazolidinone
857637-81-1

(E)-(4S,5R)-4-benzyl-3-(2'-butenoyl)-5-(1'H,1'H,2'H,2'H-perfluorooctyl)-2-oxazolidinone

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine; lithium chloride In tetrahydrofuran for 24h; Heating;87%

623-68-7Relevant articles and documents

Substrates for efficient fluorometric screening employing the NAD-dependent sirtuin 5 lysine deacylase (KDAC) enzyme

Madsen, Andreas S.,Olsen, Christian A.

experimental part, p. 5582 - 5590 (2012/09/21)

The class III lysine deacylases (KDACs), also known as the sirtuins, have emerged as interesting drug targets for therapeutic intervention in a variety of diseases. To gain a deeper understanding of the processes affected by sirtuins, the development of selective small molecule modulators of individual isozymes has been a longstanding goal. Essential for the discovery of novel modulators, however, are good screening protocols and mechanistic insights with regard to the targets in question. We therefore evaluated the activities of the seven human sirtuin hydrolases against a panel of fluorogenic substrates. Both commonly used, commercially available substrates and novel chemotypes designed to address recent developments in the field of lysine post-translational modification were evaluated. Our investigations led to the discovery of two new fluorogenic ε-N-succinyllysine-containing substrates that enable highly efficient and enzyme-economical screening employing sirtuin 5 (SIRT5). Furthermore, optimized protocols for facile kinetic investigations were developed, which should be valuable for enzyme kinetic investigations. Finally, these protocols were applied to a kinetic analysis of the inhibition of SIRT5 by suramin, a potent sirtuin inhibitor previously shown by X-ray crystallography to bind the substrate pocket of the human SIRT5 KDAC enzyme.

PROCESS FOR PRODUCING ACID ANHYDRIDE

-

Page 10-12; 14, (2008/06/13)

According to the present invention there is provided a process for producing an acid anhydride by reacting a carboxylic acid, preferably a carboxylic acid having a polymerizable group, with a sulfonyl halide compound in the presence of a tertiary amine or in the presence of a tertiary amine and an inorganic base, wherein the tertiary amine or the tertiary amine and the inorganic base are used in an amount of 0.9 to 1.2 equivalents relative to the acid generated from the sulfonyl halide compound.

COBALT(II) CHLORIDE CATALYZED SYNTHESES OF ACID ANHYDRIDES FROM ACID CHLORIDES

Srivastava, Rajiv R.,Kabalka, George W.

, p. 593 - 594 (2007/10/02)

Acid anhydrides were synthesized by reacting acid chlorides with carboxylic acids in the presence of catalytic quantities of cobalt(II) chloride.

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