HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283540Generated: October 30, 2026
Benzoyl chloride, 3,4-dichloro- → 3,4-Dichloro-N-[[1-(4-methyl-1-piperazinyl)cyclohexyl]methyl]-benzamide
https://huagongshe.com/reaction/1283540
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl chloride, 3,4-dichloro- | HCID 76403 | — |
| Reactant | 1-[1-(4-METHYLPIPERAZIN-1-YL)CYCLOHEXYL]METHANAMINE | HCID 7018132 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3,4-Dichloro-N-[[1-(4-methyl-1-piperazinyl)cyclohexyl]methyl]-benzamide | HCID 54269004 | 49.3% |
Reaction Steps
A solution of 3,4-Dichlorobenzoylchloride (1.05 g.,) in benzene (10 ml) was added dropwise over 40 mins. to a stirred solution of 1-[1-(Aminomethyl)cyclohexyl]-4-methyl piperazine (1.06 g.,) in benzene (15 ml). The mixture was heated under reflux for 1 hr. on a steambath and the solution was evaporated. The solid residue was dissolved in ethanol, acidified with ethereal HCl and evaporated to give a white solid. This solid was suspended in water, made alkaline with 5NNaOH and extracted with chloroform (x2). The combined chloroform extracts were dried (anhyd.Na2SO4) and evaporated. The solid residue was dissolved in hot petroleum ether (80°-100°) decolourised with charcoal and crystallised from petroleum ether (80°-100°) to give 1-[1-(3,4 Dichlorobenzamido methyl) cyclohexyl]-4-methyl piperazine (0.95 g; 49%) m.p. 143° -146°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03975443 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-7ce52a3ed0c24610ac21d4ddb4fae2a6 |
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| Source note | uspto-grants-1976_08 |
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