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Water → (3s,3ar,6as)-Hexahydrofuro[2,3-B]furan-3-Ol

HRID 984531
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HRID 984531 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[O:7]1[C@@H:11]2[O:12][CH2:13][CH2:14][C@H:10]2[C:9](=[O:15])[CH2:8]1.O.[OH-].[Na+]>C1COCC1>[O:7]1[C@@H:11]2[O:12][CH2:13][CH2:14][C@@H:10]2[C@H:9]([OH:15])[CH2:8]1
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참가 물질

6

반응물 4

HCID 962Water2회HCID 14798Sodium HydroxideHCID 20767149(3aR,6aS)-hexahydrofuro[2,3-b]furan-3-onHCID 21226445Aluminium lithium hydride

생성물 1

HCID 10374488(3s,3ar,6as)-Hexahydrofuro[2,3-B]furan-3-Ol수율 87.7%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매
2회

실험 절차

To a suspension of lithium aluminum hydride (15 mg) dispersed in THF (0.2 mL) was added dropwise a solution of (3aR,6aS)-hekahydrofuro[2,3-b]furan-3-on (64 mg) obtained in Example 28 in THF (0.5 mL) at 0° C. and the mixture was stirred for 1 hr. Water (0.1 mL), 15% aqueous sodium hydroxide solution (0.1 mL) and water (0.3 mL) were successively added to the reaction mixture every 30 min and the mixture was filtered and washed well with THF. The filtrate was dried over anhydrous magnesium sulfate, filtered and the solvent was evaporated to give the title compound (57 mg, 88% ee) as an oil, which was an almost pure anti-form. The spectrum data were the same as those in Example 27.

후처리

  1. filtrationthe mixture was filtered
  2. washwashed well with THF
  3. dry with materialThe filtrate was dried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-54e683b5440a47bca6db4ff96dc41dbf
출처 데이터셋
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06867321B2

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