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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448325Generated: November 3, 2026

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

https://huagongshe.com/reaction/1448325

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 numberUS04179569
Source datasetuspto-grants-1979_12
ORD IDord-07a33bbfcf4b429bb2f7bfc7b46febca
Source noteuspto-grants-1979_12