تفاعل #325801

ord-9b19e9d3744c466fb95cad467efe79e0

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with ethyl acetate (20 mL×3)
  2. 2
    غسيلThe combined organic layers were washed with brine (20 mL×3)
  3. 3
    تجفيفdried over sodium sulfate
  4. 4
    تركيزconcentrated in vacuo
  5. 5
    أخرىThe residue was purified by flash column chromatography (30% ethyl acetate in petroleum ether)

الإجراء التجريبي

To a solution of (1-bromo-6-fluoro-4-hydroxy-naphthalen-2-yl)-acetic acid methyl ester (135 mg, 0.433 mmol) in acetonitrile (4 mL) was added 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (230 mg, 0.650 mmol) at 0° C. The resulting mixture was stirred at room temperature overnight, then diluted with water (10 mL), and extracted with ethyl acetate (20 mL×3). The combined organic layers were washed with brine (20 mL×3), dried over sodium sulfate, and concentrated in vacuo. The residue was purified by flash column chromatography (30% ethyl acetate in petroleum ether) to give (1-bromo-3,6-difluoro-4-hydroxy-naphthalen-2-yl)-acetic acid methyl ester (60 mg, 42%) as a yellow solid. MS cald. for C13H9BrF2O3 330, obsd. (ESI+) [(M+H)+] 331.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08642629B2uspto-grants-2014_02