HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448084Generated: October 31, 2026
Benzhydrylpiperazine → HCID 20298863, compound
https://huagongshe.com/reaction/1448084
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzhydrylpiperazine | HCID 70048 | — |
| Reactant | 1-Chloro-4-(chloromethyl)-2-nitrobenzene | HCID 93662 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20298863 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04179505 |
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| Source dataset | uspto-grants-1979_12 |
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| ORD ID | ord-3c0aa0678e15414681f847e27bd296ae |
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| Source note | uspto-grants-1979_12 |
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