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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448306Generated: October 31, 2026

Phenethyl bromide → 4-(4-Methylanilino)-1-(2-phenylethyl)piperidine-4-carboxamide

https://huagongshe.com/reaction/1448306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantTriethylamineHCID 8471—
Reactant4-Piperidinecarboxamide, 4-[(4-methylphenyl)amino]-HCID 417239—
SolventDimethylacetamideHCID 31374—
Product4-(4-Methylanilino)-1-(2-phenylethyl)piperidine-4-carboxamideHCID 20382191—

Reaction Steps

A mixture of 33.35 parts of (2-bromoethyl)benzene, 35 parts of 4-[N-(4-methylphenyl)amino]-4-piperidinecarboxamide, 20 parts of N,N-diethylethanamine and 225 parts of N,N-dimethylacetamide is stirred for 4 hours at 70°-80° C. The reaction mixture is poured onto water and the product is extracted with trichloromethane. The extract is washed with water, dried, filtered and evaporated. The oily residue is poured onto water, whereupon the product is precipitated. It is filtered off and suspended twice in water. The product is filtered off again, washed with 2,2'-oxybispropane and dried, yielding 4-[N-(4-methylphenyl)amino]-1-(2-phenylethyl)-4-piperidinecarboxamide; mp. 163.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179569
Source datasetuspto-grants-1979_12
ORD IDord-7b5f5f6035bc433ba35a6f3ffb0b981f
Source noteuspto-grants-1979_12