HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 22760364, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | HCID 14674270 | HCID 14674270 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 22760364 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04125612 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-5e091529b244447d904618e60bc12fbc |
| Source note | uspto-grants-1978_11 |