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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973783Generated: October 31, 2026

Phenethyl bromide → Ethyl 1-phenethyl-4-(phenylamino)piperidine-4-carboxylate

https://huagongshe.com/reaction/1973783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantTriethylamineHCID 8471—
ReactantDimethylacetamideHCID 31374—
Reactant4-Piperidinecarboxylic acid, 4-(phenylamino)-, ethyl esterHCID 12298172—
SolventWaterHCID 962—
ProductEthyl 1-phenethyl-4-(phenylamino)piperidine-4-carboxylateHCID 12298147—

Reaction Steps

A mixture of 28.7 parts of (2-bromoethyl)benzene, 34.7 parts of ethyl 4-anilinoisonipecotate, 25 parts of N,N-diethylethanamine and 162 parts of N,N-dimethylacetamide is stirred for 2h. 30 at 75°-80° C. The reaction mixture is poured onto 1000 parts of water and the product is extracted three times with 210 parts of 1,1'-oxybisethane. The combined extracts are washed twice with 200 parts of water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 2% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The oily residue is crystallized from 2,2'-oxybispropane, yielding ethyl 4-(phenylamino)-1-(2-phenylethyl)-4-piperidinecarboxylate; mp. 65° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998834
Source datasetuspto-grants-1976_12
ORD IDord-e7cbba88ffc94da59c626f577891e6ac
Source noteuspto-grants-1976_12