Boron trifluoride etherate → 178167-77-6

HRID 2287457노트

반응식

HRID 2287457 반응식
[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[OH:9].B(F)(F)F.CCOCC.[CH3:19][C:20]1([CH:26]=[CH2:27])[O:25][C:23](=[O:24])[CH2:22][CH2:21]1>O1CCOCC1.CCOCC>[CH3:19][C:20]1([CH2:21][CH2:22][C:23]([OH:25])=[O:24])[CH2:26][CH2:27][C:4]2[C:3](=[C:2]([CH3:1])[C:7]([CH3:8])=[CH:6][CH:5]=2)[O:9]1

참가 물질

6

실험 절차

To a solution of 2,3-dimethylphenol (0.01 mol) and boron trifluoride diethyl etherate (0.016 mol) in dioxane (10 mL, dried on sodium) in a flask was added γ-methyl-γ-vinylbutyrolactone (0.016 mol) in dioxane (5.0 mL) via syringe pump over 50 min at 110° C. (oil bath, reflux) under nitrogen. The reaction mixture was cooled to room temperature and diluted with ether (200 mL), then washed with water (100 mL, 2×50 mL) and dried over sodium sulfate. Ether was then removed in vacuum. The residue was dissolved in methanol (30 mL), and solvent was removed in vacuum. The reaction mixture was purified by flash column chromatography on silica gel (eluent ethyl acetate/hexane, 1:1). Fractions containing the desired chroman were pooled, solvent was removed, and the compound was crystallized from ethyl acetate/hexane. M.P.: 93-94° C.

후처리

  1. temperature(oil bath, reflux) under nitrogen
  2. washwashed with water (100 mL, 2×50 mL)
  3. dry with materialdried over sodium sulfate
  4. customEther was then removed in vacuum
  5. dissolutionThe residue was dissolved in methanol (30 mL)
  6. customsolvent was removed in vacuum
  7. customThe reaction mixture was purified by flash column chromatography on silica gel (eluent ethyl acetate/hexane, 1:1)
  8. additionFractions containing the desired chroman
  9. customsolvent was removed
  10. customthe compound was crystallized from ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-3da906a38c1847e48b8d9d4c2bf41b4e
출처 데이터셋
uspto-grants-2000_07
특허 번호
US06083982

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