HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-hydroxy-N-[3-[2-(4-fluorophenylthio)-6-fluorophenyl]prop-2-enyl]urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethylsilyl isocyanate | HCID 70696 | — |
| Reactant | N-[3-[2-(4-fluorophenylthio)-6-fluorophenyl]prop-2-enyl]hydroxylamine | HCID 53877237 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-hydroxy-N-[3-[2-(4-fluorophenylthio)-6-fluorophenyl]prop-2-enyl]urea | HCID 54054261 | — |
Reaction Steps
N-[3-[2-(4-fluorophenylthio)-6-fluorophenyl]prop-2-enyl]hydroxylamine (0.91 g, 3.1 mmol) is dissolved in 16 ml of dry dioxane. Trimethylsilyl isocyanate (0.36 g, 3.1 mmol) is then added dropwise and the reaction mixture is stirred at room temperature overnight. The reaction mixture is poured into 1N HCl solution and then extracted twice with diethyl ether. The extracts are washed with water and then with brine and dried over K2CO3 to afford the crude product. Recrystallization from ethyl acetate afforded the subtitle compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05283361 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-e8a00009d2e14fceb9c1b9cccd241fb8 |
| Source note | uspto-grants-1994_02 |