تفاعل #70236

ord-5b90820628314994913bf3c02418e6c9

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةat reflux under nitrogen for 4 h
  2. 2
    تركيزThe solution was concentrated to a pale yellow oil which
  3. 3
    workup.ADDITIONwas diluted with water
  4. 4
    استخلاصThe suspension was extracted with dichloromethane (×3)
  5. 5
    غسيلThe combined organic phases were washed with water and brine
  6. 6
    تجفيفdried over magnesium sulphate
  7. 7
    ترشيحfiltered
  8. 8
    تركيزconcentrated to a white solid
  9. 9
    أخرىThe crude product was purified by column chromatography (SiO2)
  10. 10
    غسيلeluting with 95:5 petrol/ethyl acetate

الإجراء التجريبي

A solution of 3-fluoro-4-methoxyacetophenone (0.063 g, 0.377 mmol), O-(3-fluorobenzyl)hydroxylamine hydrochloride (0.100 g, 0.569 mmol) and pyridine (0.14 ml, 1.73 mmol) in ethanol (5 ml) was stirred at reflux under nitrogen for 4 h and cooled to room temperature. The solution was concentrated to a pale yellow oil which was diluted with water. The suspension was extracted with dichloromethane (×3). The combined organic phases were washed with water and brine, dried over magnesium sulphate, filtered and concentrated to a white solid. The crude product was purified by column chromatography (SiO2), eluting with 95:5 petrol/ethyl acetate, to give 3′-fluoro-4′-methoxyacetophenone-O-3-fluorobenzyloxime (CP9-126) as a white solid (0.099 g, 90%), m.p. 67°.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08536157B2uspto-grants-2013_09