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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543476Generated: October 31, 2026

Diethylcarbamoyl chloride → HCID 422755, compound

https://huagongshe.com/reaction/543476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylcarbamoyl chlorideHCID 6916—
Reactant1-(4-Chlorophenyl)piperazineHCID 97478—
SolventDichloromethaneHCID 6344—
ProductHCID 422755HCID 42275530.4%

Reaction Steps

In 40 ml of methylene chloride was dissolved 4.0 g (0.02 mole) of 1-(4-chlorophenyl)piperazine at room temperature. Then, a solution of 3.0 g (0.022 mole) of diethylcarbamoyl chloride in 30 ml off methylene chloride was dropped to the above solution over a period of 30 minutes and the mixture was stirred for 4 hours at room temperature. The precipitate was removed and the filtrate was made alkaline by addition of 30 ml of a 35% aqueous solution of sodium hydroxide and extracted with 50 ml of methylene chloride. The organic layer was dried with anhydrous sodium sulfate and the solvent was removed by distillation under reduced pressure to obtain crude 1-(4-chlorophenyl)-4-diethylcarbamylpiperazine as the residue. The low-boiling-point component was removed by distillation under reduced pressure and the residue was recrystallized from n-hexane to obtain 1.8 g of a purified product having a melting point of 63° to 64° C. The yield was 29.9%. The elementary analysis values are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04446133
Source datasetuspto-grants-1984_05
ORD IDord-bc7b48f22bfb4df4a73451729d0e6c9a
Source noteuspto-grants-1984_05