Hydrogen Peroxide → 5-Bromo-3-fluorobenzene-1,2-diol

HRID 2421580Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2421580
[OH-:1].[Na+].[Br:3][C:4]1[CH:5]=[C:6]([F:13])[C:7]([OH:12])=[C:8]([CH:11]=1)C=O.OO>S([O-])([O-])(=O)=S.[Na+].[Na+]>[Br:3][C:4]1[CH:11]=[C:8]([OH:1])[C:7]([OH:12])=[C:6]([F:13])[CH:5]=1

Komponenten

5

Versuchsvorschrift

To a 1 N aqueous solution of sodium hydroxide (230 mL, 0.23 mol), 5-bromo-3-fluoro-2-hydroxybenzaldehyde (45.0 g, 0.21 mol) was added at room temperature, and a 6% hydrogen peroxide solution (225 mL) was added dropwise over five minutes at room temperature. After the reaction mixture was stirred at room temperature for two hours, a saturated aqueous solution of sodium thiosulfate (150 mL) was added thereto at room temperature. The mixture was extracted three times with ethyl acetate (450 mL), the organic layer was washed sequentially with a 1 N aqueous solution of hydrochloric acid (150 mL) and saturated saline, dried over anhydrous magnesium sulfate, and filtered through silica gel. The solvent was distilled off from the resultant filtrate under reduced pressure to give 39.0 g of the title compound (yield: 92%).

Aufarbeitung

  1. customat room temperature
  2. extractionThe mixture was extracted three times with ethyl acetate (450 mL)
  3. washthe organic layer was washed sequentially with a 1 N aqueous solution of hydrochloric acid (150 mL) and saturated saline
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationfiltered through silica gel
  6. distillationThe solvent was distilled off from the resultant filtrate under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-ed4a3a33d62a48c89f55aa8c992854cd
Quelldatensatz
uspto-grants-2011_06
Patentnummer
US07956222B2

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