Methanol → HCID 21708319, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([N+:13]([O-])=O)[CH:5]=[C:6]([CH:9]([F:12])[CH2:10][CH3:11])[C:7]=1[Cl:8].CO.C(#N)C.O>Cl.[Cl-].[Cl-].[Cl-].[Ti+3].C(OCC)(=O)C>[Br:1][C:2]1[CH:3]=[C:4]([CH:5]=[C:6]([CH:9]([F:12])[CH2:10][CH3:11])[C:7]=1[Cl:8])[NH2:13]Participants
Procedure
6.54 g (22.1 mmol) of 3-bromo-4-chloro-5-(1-fluoropropyl)-1-nitrobenzene was dissolved in a solvent mixture comprising 30 ml of methanol and 90 ml of acetonitrile, followed by the addition of 120 ml of a 20% solution of titanium trichloride in diluted hydrochloric acid under a nitrogen stream under cooling with ice. The obtained mixture was stirred at room temperature for 3 hours and then poured into water. The resulting mixture was extratcted with ethyl acetate. The ethyl acetate phase was washed with a saturated aqueous solution of sodium hydrogen carbonate and a saturated brine successively, dried and distilled to remove the solvent. The residue was purified by silica gel column chromatography to give 5.04 g of the title compound (yield: 86%).
Workup
- temperatureunder cooling with ice
- washThe ethyl acetate phase was washed with a saturated aqueous solution of sodium hydrogen carbonate
- dry with materiala saturated brine successively, dried
- distillationdistilled
- customto remove the solvent
- customThe residue was purified by silica gel column chromatography
Sources & evidence
- ORD record
- ord-dd8750f1723f40f28a7b8ec687f497ba
- Source dataset
- uspto-grants-2001_08
- Patent number
- US06281214B1
Reaction notes
Loading…