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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437679Generated: October 29, 2026

Acetic Anhydride → HCID 21428809, compound

https://huagongshe.com/reaction/437679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 21428831HCID 21428831—
SolventWaterHCID 962—
ProductHCID 21428809HCID 21428809—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5.8 parts of 2-amino-N-{2-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]ethyl}-4-fluorobenzamide, 5.5 parts of acetic acid anhydride and 55 parts of water is stirred and heated for 30 minutes in a water-bath at about 80° C. The reaction mixture is cooled and alkalized with ammonium hydroxide. The product is extracted with trichloromethane. The aqueous phase is separated and extracted with trichloromethane. The combined organic phases are washed three times with water, dired, filtered and evaporated. The oily residue is crystallized from 4-methyl-2-pentanone. The product is filtered off and dried, yielding 4.5 parts of 2-(acetylamino)-N-{2-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]ethyl}-4-fluorobenzamide; mp. 175.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031226
Source datasetuspto-grants-1977_06
ORD IDord-2f2ac863501a463ba8360bf2a10d6a91
Source noteuspto-grants-1977_06