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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380515Generated: November 3, 2026

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

https://huagongshe.com/reaction/1380515

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 to give 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 numberUS04582833
Source datasetuspto-grants-1986_04
ORD IDord-78034706accc4d2fbc06d2b923f5f634
Source noteuspto-grants-1986_04