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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582026Generated: November 2, 2026

Benzenesulfonyl chloride → Phenylmethyl 4-[(phenylsulfonyl)oxy]-1-piperidinecarboxylate

https://huagongshe.com/reaction/1582026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
ReactantBenzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—
SolventDichloromethaneHCID 6344—
ProductPhenylmethyl 4-[(phenylsulfonyl)oxy]-1-piperidinecarboxylateHCID 8579490177%

Reaction Steps

Triethylamine (17 ml) was added dropwise to a solution of benzyl 4-hydroxy-1-piperidinecarboxylate (28.83 g) in dichloromethane (100 ml) at 0° C. and stirred for 15 minutes. Benzenesulfonyl chloride (14 ml) was added and the reaction allowed to stir at room temperature for 48 h. The mixture was washed with water (50 ml), saturated sodium bicarbonate solution (50 ml), water (50 ml) and brine (50 ml) then dried (Na2SO4), filtered and evaporated under reduced pressure. The residue was purified by chromatography (SiO2, 20% ethyl acetate in hexane to 30% ethyl acetate in hexane) to give the title compound (31.88 g, 77%) as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734189B2
Source datasetuspto-grants-2004_05
ORD IDord-20ed185898df4af38af39d9907039a4a
Source noteuspto-grants-2004_05