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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364331Generated: November 1, 2026

4-Chlorobenzenesulfonyl chloride → tert-butyl (2R)-2-{[(4-chlorophenyl)sulfonyl]amino}propanoate

https://huagongshe.com/reaction/1364331

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantTriethylamineHCID 8471—
ReactantD-Alanine tert-butyl ester hydrochlorideHCID 16211919—
SolventDichloromethaneHCID 6344—
Producttert-butyl (2R)-2-{[(4-chlorophenyl)sulfonyl]amino}propanoateHCID 6693486588.2%

Reaction Steps

To D-alanine tert-butyl ester hydrochloride (1 g) in methylene chloride (35 ml) solution, triethylamine (1.7 ml) and 4-chlorobenzenesulfonyl chloride (1.1 g) were added under ice cooling and the mixture was stirred at room temperature for 2 hours. The methylene chloride was distilled off in vacuo, then the residue was diluted with ethyl acetate. The obtained solution was successively washed with distilled water, saturated potassium hydrogensulfate aqueous solution, and saturated saline, dried over with anhydrous sodium sulfate, then concentrated. The residue was recrystallized from ethyl acetate/hexane to obtain the title compound (1.47 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888348B2
Source datasetuspto-grants-2011_02
ORD IDord-09d51251b496464d82ffe95d032e67d9
Source noteuspto-grants-2011_02