HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861223Generated: November 2, 2026
3-Fluoroaniline → 4-Amino-2-fluorophenyl thiocyanate
https://huagongshe.com/reaction/1861223
Participants
| Role | Name | HCID | Charge |
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| 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 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 |
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| Patent number | US06531470B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-18eafdac510648c4b80108b432c75657 |
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| Source note | uspto-grants-2003_03 |
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