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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892832Generated: October 30, 2026

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

https://huagongshe.com/reaction/1892832

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 numberUS08507714B2
Source datasetuspto-grants-2013_08
ORD IDord-1b4d028194824a52bbf206e10939c0b3
Source noteuspto-grants-2013_08