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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762838Generated: October 30, 2026

Ammonia → 4-(1-Acetylpiperidin-4-yl)benzenesulphonamide

https://huagongshe.com/reaction/1762838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant4-(1-Acetylpiperidin-4-yl)benzenesulphonyl chlorideHCID 20039820—
SolventEthanolHCID 702—
Product4-(1-Acetylpiperidin-4-yl)benzenesulphonamideHCID 20039833—

Reaction Steps

The product of (i) above (21.0 g) was added portionwise to a stirred mixture of concentrated aqueous ammonia solution (160 ml) and ethanol (160 ml). The mixture was warmed at 35° until solution was complete and then evaporated. The residue was triturated with water and the solid was filtered off and dried to give the title compound, (18.0 g), m.p. 196°-197° (from ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835165
Source datasetuspto-grants-1989_05
ORD IDord-72a4f3b0303c4c06ac9a418e5d4a246f
Source noteuspto-grants-1989_05