Nitric Acid → 2,2,2-Trifluoro-N-[(1S,2R)-2-hydroxy-2-(4-hydroxy-3-nitrophenyl)-1-methylethyl]acetamide

HRID 2220595Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2220595
[F:1][C:2]([F:18])([F:17])[C:3]([NH:5][C@@H:6]([CH3:16])[C@H:7]([OH:15])[C:8]1[CH:13]=[CH:12][C:11]([OH:14])=[CH:10][CH:9]=1)=[O:4].[N+:19]([O-])([OH:21])=[O:20].C(OCC)(=O)C>C(O)(=O)C>[F:1][C:2]([F:17])([F:18])[C:3]([NH:5][C@@H:6]([CH3:16])[C@H:7]([OH:15])[C:8]1[CH:13]=[CH:12][C:11]([OH:14])=[C:10]([N+:19]([O-:21])=[O:20])[CH:9]=1)=[O:4]

Komponenten

5

Versuchsvorschrift

To a solution of 2,2,2-trifluoro-N-[(1S,2R)-2-hydroxy-2-(4-hydroxyphenyl)-1-methylethyl]acetamide (26.9 g) in acetic acid (85 mL) was added dropwise 70% nitric acid (6.78 mL) at room temperature with stirring. The mixture was stirred for 15 minutes at that temperature. The resulting mixture was poured into ice-water (500 g), and ethyl acetate was added. The organic layer was separated, washed successively with saturated aqueous solution of sodium bicarbonate and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by medium-pressure liquid silica gel column chromatography (eluent: n-hexane/ethyl acetate=2/1) to afford the title compound (33.5 g).

Aufarbeitung

  1. stirringThe mixture was stirred for 15 minutes at that temperature
  2. additionwas added
  3. customThe organic layer was separated
  4. washwashed successively with saturated aqueous solution of sodium bicarbonate and brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customThe solvent was evaporated under reduced pressure
  7. customthe residue was purified by medium-pressure liquid silica gel column chromatography (eluent: n-hexane/ethyl acetate=2/1)

Quellen und Nachweise

ORD-Eintrag
ord-5791930fa1d747779f46a32650203adf
Quelldatensatz
uspto-grants-2008_08
Patentnummer
US07417169B2

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