(Trifluoromethyl)trimethylsilane → (+/-)-tert-Butyl 5-methoxy-7-methyl-4-(2,2,2-trifluoro-1-hydroxyethyl)-1H-indole-1-carboxylate

HRID 2173952Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2173952
[CH:1]([C:3]1[C:11]([O:12][CH3:13])=[CH:10][C:9]([CH3:14])=[C:8]2[C:4]=1[CH:5]=[CH:6][N:7]2[C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])=[O:2].C[Si](C)(C)[C:24]([F:27])([F:26])[F:25].CCCC[N+](CCCC)(CCCC)CCCC.[F-]>C1COCC1.[NH4+].[Cl-].[Cl-].[Na+].O>[CH3:13][O:12][C:11]1[C:3]([CH:1]([OH:2])[C:24]([F:27])([F:26])[F:25])=[C:4]2[C:8](=[C:9]([CH3:14])[CH:10]=1)[N:7]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH:6]=[CH:5]2

Komponenten

7

Versuchsvorschrift

To a solution of tert-butyl 4-formyl-5-methoxy-7-methyl-1H-indole-1-carboxylate (Example 19-D) (0.44 g, 1.52 mmol) in THF (7.24 mL), trimethyl(trifluoromethyl)silane (0.71 mL, 4.56 mmol) and then TBAF (1M in THF, 4.56 mL, 4.56 mmol) were added at 0° C., and the reaction was stirred at room temperature. After 20 minutes the reaction mixture was diluted with aq. NH4Cl and brine, extracted with EtOAc, and the organic extract was dried over MgSO4, filtered and concentrated. The resulting residue was purified by flash chromatography (0-70% EtOAc in heptanes) to provide the title compound. MS (ESI+) m/z 360.1 (M+H).

Aufarbeitung

  1. extractionextracted with EtOAc
  2. extractionthe organic extract
  3. dry with materialwas dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe resulting residue was purified by flash chromatography (0-70% EtOAc in heptanes)

Quellen und Nachweise

ORD-Eintrag
ord-ea5f183124e842c696fb0c1cbd6f2d95
Quelldatensatz
uspto-grants-2015_06
Patentnummer
US09056874B2

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