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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389296Generated: October 30, 2026

Benzhydrylpiperazine → HCID 20298863, compound

https://huagongshe.com/reaction/1389296

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 products 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 numberUS04243806
Source datasetuspto-grants-1981_01
ORD IDord-0347bec2a63e4d738d2f55ede96071e7
Source noteuspto-grants-1981_01