HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isocyanate → 1-(2,6-Dichlorobenzoyl)-3-(5-(4-(trifluoromethyl)phenyl)-3-isoxazolyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | 2,6-Dichlorobenzoyl isocyanate | HCID 12912739 | — |
| Reactant | 5-[4-(Trifluoromethyl)phenyl]-1,2-oxazol-3-amine | HCID 13035545 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(2,6-Dichlorobenzoyl)-3-(5-(4-(trifluoromethyl)phenyl)-3-isoxazolyl)urea | HCID 12960043 | — |
Reaction Steps
5-(4-(Trifluoromethyl)phenyl)-3-aminoisoxazole (500 grams) in 6 l. 1,2-dichloromethane was reacted in a reaction vessel with 2,6-dichlorobenzoyl isocyanate (567 grams). The isocyanate was added in rapid dropwise fashion over one hour keeping the temperature between 20°-40° C. The reaction mixture was allowed to react at 40° C. for three hours and was then stripped and slurried in 1 l. methanol. A white solid product formed which was filtered, dried in an air dryer, and then identified by NMR analysis as the desired compound, yield, 881 grams, m.p.=227°-230° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04336264 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-17240e3c489e43f18519349aa37c9f30 |
| Source note | uspto-grants-1982_06 |