Sodium Bisulfate → tert-Butyl {(1S)-1-methyl-2-oxo-2-[4-(trifluoromethyl)phenyl]ethyl}carbamate

HRID 985165Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 985165
CON(C)[C:4](=[O:11])[C@@H:5]([NH:7][C:8](=[O:10])[O-:9])[CH3:6].[F:13][C:14]([F:24])([F:23])[C:15]1[CH:20]=[CH:19][C:18]([Mg]Br)=[CH:17][CH:16]=1.S([O-])(O)(=O)=O.[Na+]>O1CCCC1>[F:13][C:14]([F:24])([F:23])[C:15]1[CH:20]=[CH:19][C:18]([C:4](=[O:11])[C@@H:5]([NH:7][C:8](=[O:10])[O:9][C:15]([CH3:20])([CH3:16])[CH3:14])[CH3:6])=[CH:17][CH:16]=1

Komponenten

5

Versuchsvorschrift

A solution of N-{(1S)-2-[methoxy(methyl)amino]-1-methyl-2-oxoethyl}carbamate (9.6 g) in tetrahydrofuran (180 mL) was dropwise added at 0° C. to a solution of 1.48M 4-trifluoromethylphenylmagnesium bromide in tetrahydrofuran (70 mL) which had been prepared in another batch. The mixture was stirred at room temperature for 14 hours, and cooled down to 0° C. After addition of aqueous sodium hydrogen sulfate, the reaction mixture was extracted with ethyl acetate. The organic layer was washed successively with water and brine, dried over anhydrous sodium sulfate, and filtered to remove the sodium sulfate. Evaporation of the organic solvent in vacuo gave t-butyl N-[(1S)-2-(4-trifluoromethylphenyl)-1-methyl-2-oxoethyl]carbamate (13.4 g) as an orange solid.

Aufarbeitung

  1. customhad been prepared in another batch
  2. temperaturecooled down to 0° C
  3. extractionthe reaction mixture was extracted with ethyl acetate
  4. washThe organic layer was washed successively with water and brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. customto remove the sodium sulfate
  8. customEvaporation of the organic solvent in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-d5d38341b1d5426eb138d104d6a8e0cd
Quelldatensatz
uspto-grants-2005_03
Patentnummer
US06869966B2

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