Magnesium trifluoromethanesulfonate → (R)-methyl 2-hydroxy-3-((S)-1-(triisopropylsilyloxy)propan-2-yloxy)propanoate

HRID 655725

반응식

HRID 655725 반응식
FC(F)(F)S([O-])(=O)=O.[Mg+2].FC(F)(F)S([O-])(=O)=O.[CH:18]([Si:21]([CH:30]([CH3:32])[CH3:31])([CH:27]([CH3:29])[CH3:28])[O:22][CH2:23][C@@H:24]([OH:26])[CH3:25])([CH3:20])[CH3:19].[O:33]1[CH2:35][C@@H:34]1[C:36]([O:38][CH3:39])=[O:37]>C(OCC)(=O)C>[OH:33][C@H:34]([CH2:35][O:26][C@@H:24]([CH3:25])[CH2:23][O:22][Si:21]([CH:18]([CH3:20])[CH3:19])([CH:27]([CH3:29])[CH3:28])[CH:30]([CH3:32])[CH3:31])[C:36]([O:38][CH3:39])=[O:37]

참가 물질

5

반응 조건

온도
80 °C

실험 절차

Magnesium trifluoromethanesulfonate (1.263 g, 3.92 mmol) was added to a mixture of (S)-1-(triisopropylsilyloxy)propan-2-ol (4.55 g, 19.59 mmol) and (R)-methyl oxirane-2-carboxylate (2 g, 19.59 mmol) in ethyl acetate (40 mL). The resulting suspension was heated to 80° C. for 72 hours. Further (R)-methyl oxirane-2-carboxylate (2 g, 19.59 mmol) was added and the mixture stirred at 80° C. for 48 hrs. Further (R)-methyl oxirane-2-carboxylate (2 g, 19.59 mmol) was added and the mixture stirred for 24 hrs. The mixture was allowed to cool, filtered through a bed of silica (˜10 g), washed through with EtOAc and evaporated. The crude product was purified by flash silica chromatography, elution gradient 10 to 50% EtOAc in isohexane, to afford the product (2.7 g, 41%).

후처리

  1. stirringthe mixture stirred for 24 hrs
  2. temperatureto cool
  3. filtrationfiltered through a bed of silica (˜10 g)
  4. washwashed through with EtOAc
  5. customevaporated
  6. customThe crude product was purified by flash silica chromatography, elution gradient 10 to 50% EtOAc in isohexane

출처 및 근거

ORD 기록
ord-786616f159c04a1491d48599f08480bf
출처 데이터셋
uspto-grants-2011_12
특허 번호
US08071608B2

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