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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980824Generated: October 25, 2026

Toluene → [3-Oxo-5-(o-chlorophenyl)-1-cyclohexen-1-yl]-piperazine

https://huagongshe.com/reaction/980824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPiperazineHCID 4837—
Reactant5-(2-Chlorophenyl)cyclohexane-1,3-dioneHCID 875360—
SolventWaterHCID 962—
Product[3-Oxo-5-(o-chlorophenyl)-1-cyclohexen-1-yl]-piperazineHCID 13520891—

Reaction Steps

A mixture of 24.0 g (0.108 mol) of 1,3-dioxo-5-(o-chlorophenyl)-cyclohexane, 28.4 g (0.33 mol) of anhydrous piperazine and 270 ml of toluene is heated at the boiling point under reflux for 5 hours, using a water separator. The toluene is distilled off, while still warm, in vacuo and the residue is dissolved in chloroform. This solution is extracted three times by shaking with water, to remove the excess piperazine, and dried with sodium sulphate. The concentrated solution is purified by means of column chromatography (corresponding to Example 2). Some of the fractions contain 6.5 g of the base [3-oxo-5-(o-chlorophenyl)-1-cyclohexen-1-yl]-piperazine in pure form, of melting point 159°-160° C., and another portion is still contaminated. The latter is purified by the oxalate: 6.2 g of a white salt of melting point 225°-227° C. (decomposition). After converting back into the base, a further 5.0 g are obtained. Total yield: 11.5 g (=36.7%). RF value: 0.38 (conditions corresponding to Example 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04639453
Source datasetuspto-grants-1987_01
ORD IDord-0f0735542cee4ffb8a826f62b24f6d03
Source noteuspto-grants-1987_01