Methyl 4-trimethylsilylethynylbenzoate → 4-(Trimethylsilylethynyl)benzyl alcohol

HRID 2405644

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HRID 2405644 반응식
C[O:2][C:3](=O)[C:4]1[CH:9]=[CH:8][C:7]([C:10]#[C:11][Si:12]([CH3:15])([CH3:14])[CH3:13])=[CH:6][CH:5]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[CH3:13][Si:12]([C:11]#[C:10][C:7]1[CH:6]=[CH:5][C:4]([CH2:3][OH:2])=[CH:9][CH:8]=1)([CH3:14])[CH3:15]

참가 물질

4

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온도
0 °C

실험 절차

Under argon condition, 4-((trimethylsilyl)ethynyl)benzoic acid methyl ester (316 mg, 1.36 mmol) was dissolved in 5 mL of dry THF and then cooled to 0° C. and LiAlH4 (2.04 mL, 1.0 M solution in THF, 2.04 mmol) was slowly added thereto. Upon completion of the reaction after stirring for 30 minutes at 0° C., the reaction was terminated by adding 77 μL of water, 154 μL of 10% aqueous sodium hydroxide solution and 231 μL of water in order. When the white viscous precipitate was produced, the mixture was filtered through silica pad to remove the precipitate. The resulting solution was concentrated by distillation under reduced pressure, and purified by column chromatography to obtain 258 mg (1.26 mmol, 93%) of the desired compound.

후처리

  1. customUpon completion of the reaction
  2. customthe reaction was terminated
  3. additionby adding 77 μL of water, 154 μL of 10% aqueous sodium hydroxide solution and 231 μL of water in order
  4. customWhen the white viscous precipitate was produced
  5. filtrationthe mixture was filtered through silica pad
  6. customto remove the precipitate
  7. concentrationThe resulting solution was concentrated by distillation under reduced pressure
  8. custompurified by column chromatography

출처 및 근거

ORD 기록
ord-d5ba5238ed624b6684e82be77b24e065
출처 데이터셋
uspto-grants-2014_08
특허 번호
US08809012B2

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