Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosgen toluene | HCID 19083224 | — |
| Reactant | HCID 20035714 | HCID 20035714 | — |
| Product | HCID 20035715 | HCID 20035715 | — |
Reaction Steps
To 4% phosgen-toluene solution was added 4.0 g of 2-fluoro-4-(1,1,2,2-tetrafluoroethylsulfonyl)aniline, followed by heating under reflux for 3 hours. After the completion of the reaction, the reaction mixture was concentrated to dryness under reduced pressure to give 2-fluoro-4-(1,1,2,2-tetrafluoroethylsulfonyl)phenyl isocyanate as an oily material. In 50 ml of xylene was dissolved the oily material, and 1.5 of 2.6-difluorobenzamide was added to the solution, followed by heating under reflux for 20 hours. After the completion of the reaction, the reaction mixture was cooled to 0° C., and the crystals which separated out was recovered by filtration and recrystallized from acetone to give N-(2,6-difluorobenzoyl)-N'-[2-fluoro-4-(1,1,2,2-tetrafluoroethylsulfonyl)phenyl]urea (Compound No. 5) as crystals having a melting point of 186°-187° C. The melting point of the crystals did not descend in a mixed examination with the product of Example 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04843100 |
|---|
| Source dataset | uspto-grants-1989_06 |
|---|
| ORD ID | ord-81aab2760e1a49359410599dc7215575 |
|---|
| Source note | uspto-grants-1989_06 |
|---|