HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Difluorobenzoyl isocyanate → N-(2,6-difluorobenzoyl)-N'-(2,4-difluoro-3-chloro-5-bromophenyl)-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Difluorobenzoyl isocyanate | HCID 2733369 | — |
| Reactant | 5-Bromo-3-chloro-2,4-difluoroaniline | HCID 19861634 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(2,6-difluorobenzoyl)-N'-(2,4-difluoro-3-chloro-5-bromophenyl)-urea | HCID 19861636 | — |
Reaction Steps
3.75 g of 2,6-difluorobenzoyl isocyanate are added dropwise at room temperature, with stirring, to 5 g of 2,4-difluoro-3-chloro-5-bromoaniline dissolved in 50 ml of dry toluene, and the mixture is stirred for a further 5 hours. Approximately 75% of the solvent is then removed in a rotary evaporator. The residue is diluted with hexane and the resulting precipitate is filtered off with suction, washed with hexane and dried in vacuo. The title compound of formula ##STR14## is obtained in the form of colourless crystals; m.p. 225°-227° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04910018 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-0f848796f2be48289d7bbe3350391ff7 |
| Source note | uspto-grants-1990_03 |