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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543474Generated: October 30, 2026

Diethylcarbamoyl chloride → HCID 423348, compound

https://huagongshe.com/reaction/543474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylcarbamoyl chlorideHCID 6916—
Reactant1-PhenylpiperazineHCID 7096—
SolventChloroformHCID 6212—
ProductHCID 423348HCID 42334829.5%

Reaction Conditions

Temperature40 °C

Reaction Steps

In 70 ml of chloroform was dissolved 12.0 g (0.074 mole) of 1-phenylpiperazine at room temperature, and a solution of 10.9 g (0.08 mole) of diethylcarbamoyl chloride in 30 ml of chloroform was dropped to the above solution over a period of 30 minutes. Then, the mixture was stirred at 40° C. for 5 hours and then cooled. The precipitated white crystal was removed, and the filtrate was concentrated under reduced pressure and 50 ml of a 25% aqueous solution of sodium hydroxide was added. The mixture was extracted 2 times with 50 ml of benzene and dried with anhydrous sodium sulfate. The solvent was removed by distillation to obtain crude 1-phenyl-4-diethylcarbamoylpiperazine as the residue. By distillation under reduced pressure, 5.7 g of a purified product having a boiling point of 180.5° C. at 2.3 mm Hg was obtained. The yield was 29.5%. The elementary analysis values are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04446133
Source datasetuspto-grants-1984_05
ORD IDord-416a86444ddd4642a190750fe848741f
Source noteuspto-grants-1984_05