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(2-tert-Butyloxiran-2-yl)methanol → (2R)-2,3,3-Trimethylbutane-1,2-diol

HRID 2396479
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HRID 2396479 반응식
[CH3:1][C:2]([C:5]1([CH2:8][OH:9])[CH2:7][O:6]1)([CH3:4])[CH3:3].[H-].[Al+3].[Li+].[H-].[H-].[H-]>C(OCC)C>[CH3:7][C@@:5]([OH:6])([C:2]([CH3:4])([CH3:3])[CH3:1])[CH2:8][OH:9]
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참가 물질

4

반응물 2

HCID 13446407(2-tert-Butyloxiran-2-yl)methanolHCID 21226445Aluminium lithium hydride

생성물 1

HCID 24741476(2R)-2,3,3-Trimethylbutane-1,2-diol수율 64.1%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

A solution of 2-(1,1-dimethylethyl)-2-oxiranemethanol (2.3 g, 17.7 mmol) in ethyl ether (10 ml) was added to a suspension of lithium aluminum hydride (1.477 g, 38.9 mmol) in ethyl ether (100 ml) at -5° C. and stirred at room temperature for 30 minutes. The mixture was cooled to 0° C., quenched with 10% aqueous sulfuric acid saturated with sodium sulfate. The aqueous layer was extracted with ethyl acetate and the combined extracts were washed with saturated sodium bicarbonate and brine and dried (magnesium sulfate). Concentration in vacuo followed by recrystallization from hexane gave 1.5 g of (R)-2,3,3-trimethyl-1,2-butanediol as a white solid.

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후처리

  1. temperatureThe mixture was cooled to 0° C.
  2. customquenched with 10% aqueous sulfuric acid saturated with sodium sulfate
  3. extractionThe aqueous layer was extracted with ethyl acetate
  4. washthe combined extracts were washed with saturated sodium bicarbonate and brine
  5. dry with materialdried (magnesium sulfate)
  6. concentrationConcentration in vacuo
  7. customfollowed by recrystallization from hexane

출처 및 근거

ORD 기록
ord-c30e43812ad4457eb1d9192623ee6268
출처 데이터셋
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05492910

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