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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3,4-dichloro-HCID 76403—
Reactant1-[1-(4-METHYLPIPERAZIN-1-YL)CYCLOHEXYL]METHANAMINEHCID 7018132—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product3,4-Dichloro-N-[[1-(4-methyl-1-piperazinyl)cyclohexyl]methyl]-benzamideHCID 5426900449.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03975443
Source datasetuspto-grants-1976_08
ORD IDord-7ce52a3ed0c24610ac21d4ddb4fae2a6
Source noteuspto-grants-1976_08