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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289536Generated: October 31, 2026

p-Bromobenzenesulfonyl chloride → HCID 1219636, compound

https://huagongshe.com/reaction/2289536

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
SolventDichloromethaneHCID 6344—
ProductHCID 1219636HCID 1219636—

Reaction Steps

A solution of 4-bromophenylsulphonyl chloride (7.68 g) in dichloromethane (100 ml) was added dropwise over a period of 30 minutes to a solution of 4-(ethoxycarbonyl)piperidine (4.71 g) in dichloromethane (50 ml) at 0° C. and under argon. The mixture was stirred overnight during which time it was allowed to warm to room temperature. The organic phase was washed with water, brine, dried and evaporated to give a solid. This solid was triturated in petroleum ether (bp 40-60° C.) to give 1-(4-bromophenylsulphonyl)-4-(ethoxycarbonyl)piperidine (l0.05 g), m.p. 137-133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093718
Source datasetuspto-grants-2000_07
ORD IDord-76173876f7274bdebbd9fbbde9d2aee9
Source noteuspto-grants-2000_07