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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456383Generated: November 1, 2026

N-Acetyl-L-Cysteine → HCID 57291887, compound

https://huagongshe.com/reaction/456383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Acetyl-L-CysteineHCID 12035—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-Bromobutyric acidHCID 75809—
ReactantSodium ethoxideHCID 2723922—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 57291887HCID 57291887—

Reaction Steps

A solution of 4-bromobutyric acid (5.1 g, 30.6 mmoles) and 1,1′-carbonyldiimidazol (5.61 g, 34.6 mmoles)) in chloroform (50 ml) is left at room temperature under stirring for 1 hour. To the reaction mixture N-acetyl cysteine (5 g, 30.6 mmoles) dissolved in N,N-dimethylformamide (5 ml) and sodium ethylate (50 mg) is added under stirring. After 24 hours the solution is washed with HCl 1% and brine, the organic phase is anhydrified with sodium sulphate and evaporated at reduced pressure. The obtained crude product is purified by chromatography on silica gel column, eluting with ethyl acetate/chloroform 7/3. N-acetyl-S-(4-bromobutyroyl) cysteine is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186708B2
Source datasetuspto-grants-2007_03
ORD IDord-3f77f430f45d456ca00d6aea223a2153
Source noteuspto-grants-2007_03