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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703788Generated: November 1, 2026

Piperazine → HCID 22760364, compound

https://huagongshe.com/reaction/1703788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantHCID 14674270HCID 14674270—
SolventBenzeneHCID 241—
ProductHCID 22760364HCID 22760364—

Reaction Steps

While stirring, reflux a solution of 90g of anhydrous piperazine, 52g of 4'-chloro-4-(1-chloroethyl)[1,1']biphenyl and 700 ml of anhydrous benzene for 24 hours. Add 300 ml. of water to the reaction mixture, separate the benzene layer and extract with dilute hydrochloric acid. Separate and filter the acidic aqueous phase, basify the filtrate with dilute sodium hydroxide and extract with methylene chloride. Dry the organic extract, concentrate and triturate the resulting solid residue with petroleum ether. Filter and recrystallize the product from methanol to yield 1-[1-(4'-chloro[1,1']biphenyl-4-yl)ethyl] piperazine m.p. 164°-165° C. The dihydrochloride salt (from methanol as hemihydrate) has a m.p. 263°-264°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04125612
Source datasetuspto-grants-1978_11
ORD IDord-5e091529b244447d904618e60bc12fbc
Source noteuspto-grants-1978_11