HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543474Generated: October 30, 2026
Diethylcarbamoyl chloride → HCID 423348, compound
https://huagongshe.com/reaction/543474
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylcarbamoyl chloride | HCID 6916 | — |
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 423348 | HCID 423348 | 29.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04446133 |
|---|
| Source dataset | uspto-grants-1984_05 |
|---|
| ORD ID | ord-416a86444ddd4642a190750fe848741f |
|---|
| Source note | uspto-grants-1984_05 |
|---|