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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973827Generated: November 2, 2026

Butyric anhydride → N-[4-(methoxymethyl)-1-(2-phenylethyl)-4-piperidinyl]-N-phenylbutanamide ethanedioate

https://huagongshe.com/reaction/1973827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyric anhydrideHCID 7798—
ReactantAmmonium HydroxideHCID 14923—
Reactant4-Piperidinamine, 4-(methoxymethyl)-N-phenyl-1-(2-phenylethyl)-HCID 12298210—
ProductN-[4-(methoxymethyl)-1-(2-phenylethyl)-4-piperidinyl]-N-phenylbutanamide ethanedioateHCID 12298012—

Reaction Steps

A mixture of 3 parts of 4-(methoxymethyl)-N-phenyl-1-(2-phenylethyl)-4-piperidinamine and 5 parts of butanoic acid, anhydride is stirred and refluxed for 8 hours. The reaction mixture is poured onto water and the whole is alkalized with ammonium hydroxide. The product is extracted with trichloromethane. The extract is washed with water, dried, filtered and evaporated. The oily residue is stirred in 1,1'-oxybisethane with activated charcoal. The latter is filtered off and the filtrate is evaporated. The residue is converted into the ethanedioate salt 2-propanol. The salt is filtered off and crystallized from 2-propanone, yielding 1.7 parts of N-[4-(methoxymethyl)-1-(2-phenylethyl)-4-piperidinyl]-N-phenylbutanamide ethanedioate; mp. 174.2° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998834
Source datasetuspto-grants-1976_12
ORD IDord-e7b2f4470f2347e5b5c96e42c0487cd5
Source noteuspto-grants-1976_12