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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448084Generated: October 31, 2026

Benzhydrylpiperazine → HCID 20298863, compound

https://huagongshe.com/reaction/1448084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzhydrylpiperazineHCID 70048—
Reactant1-Chloro-4-(chloromethyl)-2-nitrobenzeneHCID 93662—
SolventEthanolHCID 702—
ProductHCID 20298863HCID 20298863—

Reaction Steps

A mixture of 10.3 parts of 1-chloro-4-(chloromethyl)-2-nitrobenzene, 25.2 parts of 1-(diphenylmethyl)piperazine and 120 parts of ethanol is stirred and refluxed for 4 hours. The reaction mixture is cooled and evaporated. The residue is taken up in about 100 parts of water and the product is extracted with methylbenzene. The extract is washed with water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using trichloromethane as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from a mixture of 2,2'-oxybispropane and hexane (1:2 by volume). The product is filtered off, washed with hexane and dried, yielding 19.6 parts of 1-(4-chloro-3-nitrophenylmethyl)-4-(diphenylmethyl)piperazine; mp. 101.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179505
Source datasetuspto-grants-1979_12
ORD IDord-3c0aa0678e15414681f847e27bd296ae
Source noteuspto-grants-1979_12