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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071996Generated: October 30, 2026

Benzoyl chloride, 3,4-dichloro- → 3,4-Dichloro-N-[[1-(4-methyl-1-piperazinyl)cyclohexyl]methyl]-benzamide

https://huagongshe.com/reaction/2071996

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.Na 2 SO4) 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 numberUS04049663
Source datasetuspto-grants-1977_09
ORD IDord-024bda8ce0e7428ba5c1411f0837bbc0
Source noteuspto-grants-1977_09