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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973802Generated: October 30, 2026

Phenethyl bromide → 1-Propanone, 1-[4-(phenylamino)-1-(2-phenylethyl)-4-piperidinyl]-

https://huagongshe.com/reaction/1973802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantTriethylamineHCID 8471—
ReactantDimethylacetamideHCID 31374—
Reactant1-Propanone, 1-[4-(phenylamino)-4-piperidinyl]-HCID 12298227—
SolventWaterHCID 962—
Product1-Propanone, 1-[4-(phenylamino)-1-(2-phenylethyl)-4-piperidinyl]-HCID 12298222—

Reaction Steps

A solution of 2.7 parts of (2-bromoethyl)benzene), 3.1 parts of 1-[4-(phenylamino)-4-piperidinyl]-1-propanone and 2.6 parts of N,N-diethylethanamine in 18 parts of N,N-dimethylacetamide is stirred for 4h. 30 at 80° C. The reaction mixture is poured onto 100 parts of water and the product is extracted with benzene. The extract is washed with water, dried, filtered and evaporated. The oily residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 5% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The oily residue is crystallized from 2,2'-oxybispropane, yielding 1-[4-(phenylamino)-1-(2-phenylethyl)-4-piperidinyl]-1-propanone; mp. 105.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998834
Source datasetuspto-grants-1976_12
ORD IDord-59225f01d7c94b569e9a814b59d69817
Source noteuspto-grants-1976_12