Water → 4-Bromo-2-chloro-1-(difluoromethoxy)benzene

HRID 508451

Reaktionsgleichung

Reaktionsgleichung von HRID 508451
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([Cl:9])[CH:3]=1.O.Cl[C:12]([F:17])([F:16])C([O-])=O.[Na+].C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C=O)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH:12]([F:17])[F:16])=[C:4]([Cl:9])[CH:3]=1

Komponenten

6

Versuchsvorschrift

4-Bromo-2-chlorophenol (1.0 g, 4.8 mmol) was dissolved in DMF (35 mL) and water (5 mL) was added followed by sodium chloro(difluoro)acetate (2.0 g, 12 mmol) and cesium carbonate (3.1 g, 9.6 mmol). The mixture was stirred for 15 minutes at room temperature and then heated to 100° C. for 2 hours under nitrogen. The mixture was partitioned between water (50 mL) and TBME (50 mL). The organic phase was separated, washed brine, dried over sodium sulphate, filtered, and concentrated in vacuo. The resulting crude product was purified by silica gel chromatography eluting with 0 to 30% EtOAc in heptane to afford the title compound as colourless oil (0.83 g, 67%).

Aufarbeitung

  1. temperatureheated to 100° C. for 2 hours under nitrogen
  2. customThe mixture was partitioned between water (50 mL) and TBME (50 mL)
  3. customThe organic phase was separated
  4. washwashed brine
  5. dry with materialdried over sodium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe resulting crude product was purified by silica gel chromatography
  9. washeluting with 0 to 30% EtOAc in heptane

Quellen und Nachweise

ORD-Eintrag
ord-9203e8e24d5f4596b4d18b91e4a06e90
Quelldatensatz
uspto-grants-2015_08
Patentnummer
US09096500B2

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