반응 #70420

ord-c78bc94182cb42c48b59f4800f97a3c8

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출extracted with ethyl acetate
  2. 2
    세척The organic layer was washed with brine
  3. 3
    건조dried over anhydrous sodium sulfate
  4. 4
    농축concentrated under reduced pressure
  5. 5
    기타The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1)

실험 절차

A solution of 2,5-dibromopyridine (474 mg, 2.00 mmol) and 4-(methanesulfonyl)benzyl alcohol (372 mg, 2.00 mmol) in tetrahydrofuran (5 mL) was cooled to −15° C. under N2 and potassium tert-butoxide (1.0M in tetrahydrofuran, 2.2 mL, 2.20 mmol) was added dropwise over 10 minutes. The mixture was stirred at 0° C. for 5.5 hours, poured into saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1) to give the title compound (210 mg, yield 31%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08536176B2uspto-grants-2013_09