HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 1-Trifluoromethyl-3-(4'-fluorophenyl)-3-hydroxyurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Benzenamine, 4-fluoro-N-hydroxy- | HCID 164595 | — |
| Reactant | Trifluoromethyl isocyanate | HCID 12494313 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Trifluoromethyl-3-(4'-fluorophenyl)-3-hydroxyurea | HCID 21553686 | — |
Reaction Steps
p-Fluoronitrobenzene (14.1 grams; 0.1 mol) is dissolved in tetrahydrofuran (100 ml). Ten percent palladium on charcoal catalyst (0.1 gram) is added to the solution followed by hydrazine (6.0 ml; 0.1 mol), and the resulting mixture stirred at room temperature for about 48 hours with cooling as necessary. The reaction mixture, containing N-(4-fluorophenyl)hydroxylamine, is dried over anhydrous magnesium sulfate and filtered. To this solution is added trifluoromethyl isocyanate (11.1 grams; 0.1 mol) and the solution is stirred for about 15 minutes. The reaction mixture is concentrated by evaporation of solvent and the resulting precipitate is recovered by filtration to yield 1-trifluoromethyl-3-(4'-fluorophenyl)-3-hydroxyurea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03944410 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-0602c3d4e9bc4c668329009b7e253eb4 |
| Source note | uspto-grants-1976_03 |