Ethanol → 3-Bromo-5-(2,4-difluorophenoxy)aniline
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:14]=[C:15]([N+:17]([O-])=O)[CH:16]=1)[O:5][C:6]1[CH:11]=[CH:10][C:9]([F:12])=[CH:8][C:7]=1[F:13].[Cl-].[NH4+].O.C(O)C>C1COCC1.[Fe]>[Br:1][C:2]1[CH:16]=[C:15]([CH:14]=[C:4]([O:5][C:6]2[CH:11]=[CH:10][C:9]([F:12])=[CH:8][C:7]=2[F:13])[CH:3]=1)[NH2:17]Participants
Procedure
A mixture of 1-(3-bromo-5-nitrophenoxy)-2,4-difluorobenzene (54 mg, 0.16 mmol), ammonium chloride (18 mg, 0.32 mmol), and iron powder (45 mg, 0.80 mmol) suspended in THF (300 uL), water (100 uL) and ethanol (300 uL) was heated to 100° C. using microwave irradiation (normal) for 3 h. The crude reaction mixture was filtered through a short plug of celite; the celite plug was washed with MeOH (˜5 mL). The resulting filtrate was concentrated in vacuo. The resulting residue was diluted with EtOAc (50 ml) and washed with saturated bicarbonate solution (aq), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude solid was purified by silica gel column chromatography using a gradient of EtOAc (5 to 20%) in hexanes to afford the title compound (48 mg, 100%) as a yellow solid. LCMS (M+H)+=301.
Workup
- custommicrowave irradiation (normal) for 3 h
- customThe crude reaction mixture
- filtrationwas filtered through a short plug of celite
- washthe celite plug was washed with MeOH (˜5 mL)
- concentrationThe resulting filtrate was concentrated in vacuo
- additionThe resulting residue was diluted with EtOAc (50 ml)
- washwashed with saturated bicarbonate solution (aq)
- dry with materialdried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe crude solid was purified by silica gel column chromatography
Sources & evidence
- ORD record
- ord-5e0bcb8ddbf143418b7b9399c9e5f58e
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09034900B2
Reaction notes
Loading…