HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280852Generated: October 29, 2026
Benzoyl chloride → HCID 23320196, compound
https://huagongshe.com/reaction/280852
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | HCID 19370338 | HCID 19370338 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 23320196 | HCID 23320196 | — |
Reaction Steps
To a solution of 1-(3-aminopropyl)-4-(4-chlorobenzhydryl)piperazine (1.7 g) and triethylamine (0.7 g) in chloroform (20 ml) was dropwise added benzoyl chloride (0.7 ml) at ambient temperature and the mixture was stirred at the same temperature for 1.5 hours. The reaction mixture was washed successively with aqueous sodium bicarbonate and water, and then extracted with 10% hydrochloric acid. After neutralizing the aqueous extract with aqueous sodium carbonate, the desired product was extracted with ethyl acetate. The organic extract was washed with water, dried and evaporated in vacuo to give an oil. According to a conventional manner, the oily product was converted to fumaric acid salt, which was recrystallized from a mixture of ethanol and diethyl ether to afford 1-(3-benzoylaminopropyl)-4-(4-chlorobenzhydryl)piperazine fumarate (0.82 g) as white crystals. mp: 173°-175° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04591590 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-5268feb9bfec4d1d9eb5919a79aa3ba7 |
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| Source note | uspto-grants-1986_05 |
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