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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dichlorobenzyl chloride | HCID 7609 | — |
| Reactant | 1-Piperazinecarboxylic acid, ethyl ester | HCID 8431 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 1-(3,4-Dichlorobenzyl)piperazine | HCID 2758074 | 19% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04562189 |
|---|
| Source dataset | uspto-grants-1985_12 |
|---|
| ORD ID | ord-66e48b2487ed474c96b677a8f19d943f |
|---|
| Source note | uspto-grants-1985_12 |
|---|