Methanol → HCID 21708319, compound

HRID 651405Notes

Reaction equation

HRID 651405 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

8

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

  1. temperatureunder cooling with ice
  2. washThe ethyl acetate phase was washed with a saturated aqueous solution of sodium hydrogen carbonate
  3. dry with materiala saturated brine successively, dried
  4. distillationdistilled
  5. customto remove the solvent
  6. 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

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