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-difluoroaniline (25g) and 25.2 g of pyridine were dissolved in 200 ml of dichloromethane to which was added dropwise 33.3 g of phenyl chloroformate with ice cooling. After stirring for 30 minutes with ice cooling, the reaction solution was washed with water and dried followed by distilling the solvent to give a mixture of phenyl 2,4-difluorophenylcarbamate and pyridine. To the mixture was added 30.7 g of 2-(di-ethoxy)ethylamine and the mixture was stirred at room temperature. The crystals separated out were filtered 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 | US05466820 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-458278adf92941f1a13d84297af8e95b |
| Source note | uspto-grants-1995_11 |