HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389312Generated: November 1, 2026
Benzhydrylpiperazine → HCID 20298725, compound
https://huagongshe.com/reaction/1389312
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzhydrylpiperazine | HCID 70048 | — |
| Reactant | 2-Bromo-1-(4-chloro-3-nitrophenyl)ethan-1-one | HCID 2778330 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 20298725 | HCID 20298725 | — |
Reaction Steps
A mixture of 13.9 parts of 1-(diphenylmethyl)piperazine, 8.35 parts of 2-bromo-1-(4-chloro-3-nitrophenyl)ethanone and 40 parts of 2-propanone is stirred for 30 minutes at room temperature. The formed precipitate is filtered off and 210 parts of 2,2'-oxybispropane are added to the filtrate. The whole is treated with activated charcoal. The latter is filtered off and an excess of 2-propanol, previously saturated with gaseous hydrogen chloride, is added to the filtrate. The formed hydrochloride salt is filtered off, stirred in 80 parts of 2-propanol, filtered off again and crystallized from ethanol. The product is filtered off and recrystallized from 2-methoxyethanol, yielding 6.4 parts of 1-(4-chloro-3-nitrophenyl)-2-[4-(diphenylmethyl)-1-piperazinyl]ethanone dihydrochloride; mp. 165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04243806 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-80e2322f21844fcc833bb01df9814cdb |
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| Source note | uspto-grants-1981_01 |
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