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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656321Generated: October 27, 2026

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

https://huagongshe.com/reaction/656321

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 numberUS08071624B2
Source datasetuspto-grants-2011_12
ORD IDord-d165c8a71e7d4f48b27d35b029d9dec2
Source noteuspto-grants-2011_12