HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(2,2-diethoxyethyl)-N'-(2,4-difluorophenyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,4-Difluoroaniline | HCID 9709 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | phenyl N-(2,4-difluorophenyl)carbamate | HCID 13733129 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2,2-diethoxyethyl)-N'-(2,4-difluorophenyl)urea | HCID 19065111 | — |
Reaction Steps
2,4-Difluroaniline (25 g) and 25.2 g of pyridine were dissolved in 200 ml of dichloromethane and, with ice cooling, 33.3 g of phenyl chloroformate was added dropwise thereinto. The reaction solution was stirred with ice cooling for 30 minutes, washed with water and dried. The solvent was distilled off to give a mixture of phenyl 2,4-difluorophenylcarbamate and pyridine. To the mixture was added 30.7 g of 2-(diethoxy)ethylamine, and the resulting mixture was stirred at room temperature. The crystals separated out were collected by filtration and washed with petroleum ether to give 37.8 g of N-(2,2-diethoxyethyl)-N'-(2,4-difluorophenyl)urea as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05545652 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-09a2bdf6791a4784a8241e1c00141757 |
| Source note | uspto-grants-1996_08 |