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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412392Generated: October 25, 2026

Sodium Hydroxide → (4-Benzylpiperazin-1-yl)(cyclohexyl)methanone

https://huagongshe.com/reaction/2412392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantCyclohexanecarbonyl chlorideHCID 75938—
Reactant1-BenzylpiperazineHCID 75994—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product(4-Benzylpiperazin-1-yl)(cyclohexyl)methanoneHCID 56273874%

Reaction Steps

To a solution of 21.2 g (0.12 mole) of 1-benzylpiperazine in 100 ml of CHCl3 was added dropwise over a period of 30 minutes a solution of 15.0 g (0.10 mole) of cyclohexanecarbonyl chloride in 50 ml of CHCl3. The mixture was allowed to stand at room temperature during 45 minutes and was made basic with 5 g of sodium hydroxide in 50 ml of water. The nonaqueous layer was separated, dried over sodium sulphate and concentrated. The residue was distilled b.p. 150°-56° C. at 0.1-0.2 mmHg to give 21.2 g of 1-cyclohexanecarbonyl-4-benzylpiperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04492698
Source datasetuspto-grants-1985_01
ORD IDord-2f49ef55eced435db77d406044c58ef4
Source noteuspto-grants-1985_01