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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073252Generated: October 27, 2026

4-Chlorobenzenesulfonyl chloride → (2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-methoxycarbonylpyrrolidine

https://huagongshe.com/reaction/2073252

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantTriethylamineHCID 8471—
Reactant1-tert-butyl 2-methyl (2S,4R)-4-aminopyrrolidine-1,2-dicarboxylateHCID 7009918—
SolventDichloromethaneHCID 6344—
Product(2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-methoxycarbonylpyrrolidineHCID 1477268588.2%

Reaction Steps

To a solution of (2S,4R)-4-amino-1-t-butoxycarbonyl-2-methoxycarbonylpyrrolidine (6.04 g) in dichloromethane (60 ml) were added triethylamine (3.44 ml) and p-chlorobenzenesulfonyl chloride (6.26 g) in an ice bath. After being stirred at room temperature overnight, the solution was washed successively with diluted hydrochloric acid, saturated aqueous sodium bicarbonate and brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was crystallized from n-hexane to give (2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-methoxycarbonylpyrrolidine (9.13 g) as a pale yellow crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04916152
Source datasetuspto-grants-1990_04
ORD IDord-6ada3590b824473e90e302a21ed24dde
Source noteuspto-grants-1990_04