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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220205Generated: October 30, 2026

2-Chlorobenzenesulfonyl chloride → 1-(2-Chloro-benzenesulfonyl)-piperidine-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/220205

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzenesulfonyl chlorideHCID 76187—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl piperidine-3-carboxylate--hydrogen chloride (1/1)HCID 12896004—
SolventDichloromethaneHCID 6344—
Product1-(2-Chloro-benzenesulfonyl)-piperidine-3-carboxylic acid ethyl esterHCID 386201086.4%

Reaction Steps

To a solution of 3.87 g piperidine-3-carboxylic acid ethyl ester hydrochloride (commercially available) (20 mmol) in 40 mL DCM was added 10 mL of DIPEA (60 mmol). At room temperature 2.72 mL 2-chloro-benzenesulfonyl chloride (20 mmol) was added drop wise and stirred for 14 h. The mixture was diluted with 30 mL of DCM, washed with water (3×50 mL) and the organic layer was dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to obtain the crude product which was further purified by column chromatography on silica eluting with 10% ethyl acetate in hexane to yield 5.73 g (86.3%) of the title compound. (MH+) 332.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202888B2
Source datasetuspto-grants-2012_06
ORD IDord-decf172425a84e979d2d2cd63b4c8015
Source noteuspto-grants-2012_06