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3-Furancarboxylic acid, 2,5-dimethyl-, methyl ester → (2,5-Dimethylfuran-3-yl)methanol

HRID 1581479
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HRID 1581479 반응식
[CH3:1][C:2]1[O:3][C:4]([CH3:11])=[CH:5][C:6]=1[C:7](OC)=[O:8].[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[CH3:1][C:2]1[O:3][C:4]([CH3:11])=[CH:5][C:6]=1[CH2:7][OH:8]
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참가 물질

4

반응물 2

HCID 802483-Furancarboxylic acid, 2,5-dimethyl-, methyl esterHCID 21226445Aluminium lithium hydride

생성물 1

HCID 10396847(2,5-Dimethylfuran-3-yl)methanol수율 94%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

To a 0° C. solution of methyl 2,5-dimethyl-3-furanoate (2.0 g, 13.0 mmol) in THF (130 mL) under N2 was added lithium aluminum hydride (39 mL of a 1.0 M solution in THF, 38.9 mmol) dropwise. The reaction was stirred at 0° C. for 3.5 h, at which time it was quenched cautiously with saturated aqueous Na2SO4 solution and allowed to warm to room temperature. The reaction mixture was filtered and rinsed with ethyl acetate, the filtrate was diluted with more ethyl acetate and the layers separated. The organic layer was washed with saturated aqueous NH4Cl, water and brine and dried over Na2SO4. The solution was filtered and concentrated to afford the title compound as a clear liquid (1.54 g, 12.2 mmol, 94%). 1H NMR (300 MHz, DMSO-d6): δ 5.93 (s, 1H); 4.18 (s, 2H); 2.17 (s, 3H); 2.15 (s, 3H).

후처리

  1. customwas quenched cautiously with saturated aqueous Na2SO4 solution
  2. temperatureto warm to room temperature
  3. filtrationThe reaction mixture was filtered
  4. washrinsed with ethyl acetate
  5. additionthe filtrate was diluted with more ethyl acetate
  6. customthe layers separated
  7. washThe organic layer was washed with saturated aqueous NH4Cl, water and brine
  8. dry with materialdried over Na2SO4
  9. filtrationThe solution was filtered
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-a082dcb31e2f4069aed6afecb3ac8471
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06730675B2

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