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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973809Generated: October 29, 2026

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

https://huagongshe.com/reaction/1973809

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 numberUS03998834
Source datasetuspto-grants-1976_12
ORD IDord-2971d27e840949f085a11b8a15582bb3
Source noteuspto-grants-1976_12