반응 #77561

ord-44d6565d2ae8422c8393a77b123d9947

반응 방정식

O
Water
COc1cc(O)cc(OC)c1
3,5-dimethoxyphenol
c1c[nH]cn1
imidazole
CC(C)(C)[Si](Cl)(c1ccccc1)c1ccccc1
t-butylchlorodiphenylsilane
COc1cc(OC)cc(O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)c1
1-t-butyldiphenylsiloxy-3,5-dimethoxybenzene
수율 94.1%

반응 조건

온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출the mixture was extracted with ethyl acetate-hexane (1:2)
  2. 2
    세척The organic layer was washed with water
  3. 3
    건조dried over anhydrous sodium sulfate
  4. 4
    농축concentrated under reduced pressure
  5. 5
    기타The residue was purified by column chromatography on silica gel

실험 절차

To a solution of 3,5-dimethoxyphenol (6.73 g, 43.7 mmol) in anhydrous dimethylformamide (50 mL) were added imidazole (5.95 g, 87.4 mmol) and t-butylchlorodiphenylsilane (15.0 g, 54.6 mmol), and the mixture was stirred at 50° C. for 4 hours. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate-hexane (1:2). The organic layer was washed with water, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel to yield 1-t-butyldiphenylsiloxy-3,5-dimethoxybenzene as a colorless crystalline powder (melting point: 95.5-96.5° C.) (16.14 g, yield: 94%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06706703B2uspto-grants-2004_03