Reaktion #159748

ord-2baf83ea5cbc462398226698f40c2d28

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigequenched by the addition of aq. NaHCO3 (10 mL)
  2. 2
    SonstigeThe volatiles were evaporated under reduced pressure
  3. 3
    Extraktionthe resulting mixture was extracted with dichloromethane (2×20 mL)
  4. 4
    Waschenwashed with brine (5 mL)
  5. 5
    Trocknendried over sodium sulfate
  6. 6
    Einengenconcentrated
  7. 7
    Sonstigewas purified by silica gel column chromatography

Vorschrift

To a stirred solution of 1-[6-(5-bromo-2-chloro-benzoyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone (1.0 g, 2.23 mmol) in 1:2 of 1,2-dichloroethane/MeCN (12 mL) was added Et3SiH (0.755 mL, 4.68 mmol) and BF3.OEt2 (0.34 mL, 2.90 mmol) simultaneously at 20° C. The reaction mixture was heated at 50° C. for 4 h and quenched by the addition of aq. NaHCO3 (10 mL). The volatiles were evaporated under reduced pressure; the resulting mixture was extracted with dichloromethane (2×20 mL), washed with brine (5 mL), dried over sodium sulfate, concentrated and was purified by silica gel column chromatography to furnish 1-[6-(5-bromo-2-chloro-benzyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone (0.60 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08828951B2uspto-grants-2014_09