HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-Bromo-4-fluoroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 2-Bromo-1-fluoro-4-nitrobenzene | HCID 69699 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Bromo-4-fluoroaniline | HCID 2779286 | 92% |
Reaction Steps
2-Bromo-1-fluoro-4-nitrobenzene was dissolved in tetrahydrofuran (75 mL) and ethanol (75 mL) and tin(II) chloride dihydrate added and the mixture left to stir at ambient temperature for 4 h. The solvent was evaporated and the residue was treated with ice-cold 2 N sodium hydroxide solution (200 mL). The resulting slurry was stirred for 30 min then extracted with dichloromethane (3×200 mL). The combined organic phase was washed with water (200 mL) and brine (200 mL), dried over anhydrous magnesium sulfate, filtered and evaporated to give 3-bromo-4-fluorophenylamine (7.92 g, 92%) as a yellow oil: δH (360 MHz, CDCl3) 3.53 (2H, s), 6.53-6.57 (1H, m), 6.83-6.85 (1H, m), 6.90 (1H, dd, J 9 and 9).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06960598B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-c07c63d4dd2b44b88f4a91c27ce12326 |
| Source note | uspto-grants-2005_11 |