HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → N-Phenyl-N'-(trifluoromethyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Trifluoromethyl isocyanate | HCID 12494313 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-Phenyl-N'-(trifluoromethyl)urea | HCID 21511693 | — |
Reaction Steps
A solution of aniline (93.12 grams; 1.0 mol) in toluene (200 ml) is charged into a glass reaction flask equipped with a mechanical stirrer, thermometer and gas inlet tube. Trifluoromethyl isocyanate (111 grams; 1.0 mol) is slowly bubbled into the reaction medium with vigorous stirring. The temperature of the reaction mixture is kept below about 50° C. After the addition is completed the reaction mixture is stirred for an additional period of about 1 hour. After this time the toluene is stripped from the reaction mixture under reduced pressure. The residue is then recrystallized to yield N-phenyl-N'-trifluoromethyl urea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03982019 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-00be095e60074bec9eb2b08e9e7517e9 |
| Source note | uspto-grants-1976_09 |