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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → (3s,3ar,6as)-Hexahydrofuro[2,3-B]furan-3-Ol

HRID 984531
ノート
印刷プレビュー

反応式

HRID 984531 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962Water2 回HCID 14798Sodium HydroxideHCID 20767149(3aR,6aS)-hexahydrofuro[2,3-b]furan-3-onHCID 21226445Aluminium lithium hydride

生成物 1

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

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒
2 回

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-54e683b5440a47bca6db4ff96dc41dbf
出典データセット
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06867321B2

反応ノート

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