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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065449Generated: October 30, 2026

Benzenesulfonyl chloride → Ethyl 1-(phenylsulfonyl)piperidine-3-carboxylate

https://huagongshe.com/reaction/2065449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
ReactantEthyl nipecotateHCID 98969—
SolventDichloromethaneHCID 6344—
ProductEthyl 1-(phenylsulfonyl)piperidine-3-carboxylateHCID 290453494.6%

Reaction Steps

A mixture of ethyl piperidine-3-carboxylate (1.00 g, 6.36 mmol), benzenesulfonyl chloride (0.812 mL, 6.36 mmol), and triethylamine (2.66 mL, 19.1 mmol) in methylene chloride (10.0 mL) was stirred at r.t. for 2 hours. The mixture was quenched with water, then extracted with ethyl acetate. The extract was washed with 1N HCl solution, water, sat'd sodium bicarbonate solution, water, and brine, successively. Then, the extract was dried over sodium sulfate (anhydrous). After filtration, the filtrate was concentrated to yield 1.79 g (94%) of ethyl 1-(phenylsulfonyl)piperidine-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288417B2
Source datasetuspto-grants-2012_10
ORD IDord-1766c511f13d42be9fe335eb6a526980
Source noteuspto-grants-2012_10