تفاعل #317331

ord-d3fe3a7b38454c21928968008ef4e53d

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction was quenched by addition of of 60 mL of 2M H2SO4
  2. 2
    استخلاصThe reaction mixture was extracted with 40 mL 50 mL EtOAc
  3. 3
    workup.ADDITIONthe aqueous phase was basified by addition 12 mL of 5M NaOH
  4. 4
    استخلاصThe aqueous phase was then extracted twice with 70 mL of EtOAc
  5. 5
    غسيلthe combined organic layers were washed with water
  6. 6
    تجفيفdried (MgSO4)
  7. 7
    أخرىThe MgSO4 was removed by filtration and solvent
  8. 8
    أخرىwas removed under reduced pressure
  9. 9
    أخرىThe residue was purified by flash chromatography (40 mm×15 cm) with hexanes/EtOAc (0:1 to 4:1)

الإجراء التجريبي

2-Methoxyphenyl magnesium bromide (53.3 mL of 1.75 M solution in THF was cooled to 0° C. 3,5-Difluoronicotinonitrile (5.0 g, 35.6 mmol) was added over 20 minutes to the reaction mixture at 0° C. The reaction was quenched by addition of of 60 mL of 2M H2SO4, and the mixture was allowed to warm to room temperature. The reaction mixture was extracted with 40 mL 50 mL EtOAc, and the aqueous phase was basified by addition 12 mL of 5M NaOH. The aqueous phase was then extracted twice with 70 mL of EtOAc, and the combined organic layers were washed with water, and dried (MgSO4). The MgSO4 was removed by filtration and solvent was removed under reduced pressure. The residue was purified by flash chromatography (40 mm×15 cm) with hexanes/EtOAc (0:1 to 4:1) to yield 7.9 g of (3,5-difluoro-pyridin-2-yl)-(2-methoxy-phenyl)-methanone. Mass Spec. M+H=250.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07566708B2uspto-grants-2009_07