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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834709Generated: October 31, 2026

Piperidine → N-(2-chloroethyl)benzenesulfonamide

https://huagongshe.com/reaction/1834709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantSulfuryl chlorideHCID 24648—
ReactantN-(2-hydroxyethyl)benzenesulfonamideHCID 1722145—
CatalystCarbon TetrachlorideHCID 5943—
ProductN-(2-chloroethyl)benzenesulfonamideHCID 4562550—

Reaction Steps

40.2 of N-(β-hydroxyethyl)-benzene sulfonamide was slurried in 100 ml. of carbon tetrachloride containing 5 drops of piperidine. Then, 47.6 g. of sulfonyl chloride was added over 10 minutes, keeping the temperature at 20°-25° C. during the addition. The reaction was completed by heating on a steam bath for one hour. The mixture was concentrated on the steam bath, dissolved in benzene and washed twice with dilute aqueous solution of sodium chloride, dried over magnesium sulfate, filtered and the benzene evaporated on the steam bath with air. The product was crystallized from benzene cyclohexane to yield 28.0 g. of product, m.p. 58°-62° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04071349
Source datasetuspto-grants-1978_01
ORD IDord-985ec50cb34342228281cf693ce31418
Source noteuspto-grants-1978_01