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3-Methyl-3-(5-methyl-furan-2-yl)-butyric acid methyl ester → 3-Methyl-3-(5-methyl-furan-2-yl)-butan-1-ol

HRID 1807022
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인쇄 미리보기

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HRID 1807022 반응식
C[O:2][C:3](=O)[CH2:4][C:5]([CH3:13])([C:7]1[O:8][C:9]([CH3:12])=[CH:10][CH:11]=1)[CH3:6].[H-].[H-].[H-].[H-].[Li+].[Al+3]>O1CCCC1>[CH3:13][C:5]([C:7]1[O:8][C:9]([CH3:12])=[CH:10][CH:11]=1)([CH3:6])[CH2:4][CH2:3][OH:2]
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참가 물질

4

반응물 2

HCID 143572913-Methyl-3-(5-methyl-furan-2-yl)-butyric acid methyl esterHCID 21226445Aluminium lithium hydride

생성물 1

HCID 149615083-Methyl-3-(5-methyl-furan-2-yl)-butan-1-ol수율 91.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

Step D To a solution of 3-methyl-3-(5-methyl-furan-2-yl)-butyric acid methyl ester (1.5 g, 7.8 mmol) in anhydrous tetrahydrofuran (50 mL) at 0° C. was added a tetrahydrofuran solution (1 M) of LiAlH4 (10 mL, 10 mmol) under nitrogen. The reaction mixture was stirred at 0° C. for 1 h, then poured into a ice-water. The mixture was extracted with ethyl acetate. The organic layer were separated, washed with water, aqueous HCl solution, brine, dried over MgSO4, and concentrated to give 3-methyl-3-(5-methyl-furan-2-yl)-butan-1-ol as a yellow oil (1.2 g, 77%).

후처리

  1. extractionThe mixture was extracted with ethyl acetate
  2. customThe organic layer were separated
  3. washwashed with water, aqueous HCl solution, brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-c8ef4063fadc4bba819f15fdfb1f6086
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08354444B2

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