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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638533Generated: October 25, 2026

3,4-Dichlorobenzyl chloride → 1-(3,4-Dichlorobenzyl)piperazine

https://huagongshe.com/reaction/638533

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichlorobenzyl chlorideHCID 7609—
Reactant1-Piperazinecarboxylic acid, ethyl esterHCID 8431—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium HydroxideHCID 14797—
SolventEthanolHCID 702—
SolventO-XyleneHCID 7237—
Product1-(3,4-Dichlorobenzyl)piperazineHCID 275807419%

Reaction Steps

A mixture of 39.0 g (0.2 moles) of 3,4-dichlorobenzyl chloride, 31.6 g (0.2 moles) of ethyl N-piperazinocarboxylate, 22.0 g (0.21 moles) of anhydrous sodium carbonate and 200 ml of xylene was refluxed for 3 hours using a Dean-Stark trap. Then the mixture was stirred at room temperature for 16 hours, filtered and washed with xylene. The filtrate was evaporated in vacuo and gave a syrup. A 750 ml amount of 4N potassium hydroxide in 95% ethanol was added to the syrup and the mixture was refluxed for 18 hours. The reaction mixture was evaporated to a paste and 250 ml of water was added. The solution was extracted twice with 250 ml of chloroform. The extracts were combined, dried over magnesium sulfate and filtered. The filtrate was evaporated in vacuo and gave a syrup. The syrup was distilled, bp 132°-135° C./0.05 mm of mercury and gave 9.3 g of 1-(3,4-dichlorobenzyl)piperazine as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04562189
Source datasetuspto-grants-1985_12
ORD IDord-66e48b2487ed474c96b677a8f19d943f
Source noteuspto-grants-1985_12