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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762837Generated: October 30, 2026

Chlorosulfonic acid → 4-(1-Acetylpiperidin-4-yl)benzenesulphonyl chloride

https://huagongshe.com/reaction/1762837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantHCID 11608128HCID 11608128—
Product4-(1-Acetylpiperidin-4-yl)benzenesulphonyl chlorideHCID 20039820—

Reaction Steps

1-Acetyl-4-phenylpiperidine, [Chem. Abs., 75, 5728b (1971] (16.30 g) was added portionwise over 1 hour to stirred chlorosulphonic acid (53.3 ml) at 0°. The solution was stirred at 0° for 1 hour, then at room temperature for 2 hours, and then finally poured cautiously onto an excess of ice. When the ice had melted the mixture was extracted several times with dichloromethane. The combined organic extracts were washed with water, dried (Na2SO4) and evaporated to give the title compound, (23.0 g), m.p. 133°-134°, used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835165
Source datasetuspto-grants-1989_05
ORD IDord-7758a8711e374a31a578e2d63a02b74d
Source noteuspto-grants-1989_05