HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Fluoroaniline → 4-Amino-2-fluorophenyl thiocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Fluoroaniline | HCID 9742 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Amino-2-fluorophenyl thiocyanate | HCID 22245079 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
N-Bromosuccinimide (1.76 g, 9.89 mmol) and potassium thiocyanate (1.75 g, 18.0 mmol) in methanol (30 ml) were stirred for 15 minutes at room temperature. The reaction mixture was cooled to 0° C., and 3-fluoroaniline (1.00 g, 9.0 mmol) was added dropwise. The mixture was stirred at 0° C. for 2 h. Solvent was removed under vacuum, and the residue was washed with dichloromethane. The mixture was filtered to remove succinimide by-product, and the solution was washed with water, brine, and dried (MgSO4). Solvent was removed under vacuum to afford the desired product as a colorless oil. Yield 1.45 g (96%). 1H NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562844B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-0412ebc0ca3f4c9c8e682af7ba4d1677 |
| Source note | uspto-grants-2003_05 |