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Sodium borohydride → HCID 53944516、化合物

HRID 726177
ノート
印刷プレビュー

反応式

HRID 726177 の反応式
[CH3:1][O:2][C:3]([C:5]1[CH:6]=[CH:7][CH:8]=[C:9]2[C:14]=1[S:13][CH2:12][CH2:11][C:10]2=[O:15])=[O:4].[BH4-].[Na+]>C(O)C>[CH3:1][O:2][C:3]([C:5]1[CH:6]=[CH:7][CH:8]=[C:9]2[C:14]=1[S:13][CH2:12][CH2:11][CH:10]2[OH:15])=[O:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 4311764Sodium borohydrideHCID 130039219HCID 130039219、化合物

生成物 1

HCID 53944516HCID 53944516、化合物収率 99%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Methylthiochroman-4-one-8-carboxylate (0.500 g, 2.25mmol) was dissolved with stirring in ethanol (20 ml) and treated with sodium borohydride (0.085 g, 2.25 mmol). After 1 h, the reaction mixture was evaporated under reduced pressure and the residue partitioned between ethyl acetate and water. The aqueous layer was then extracted with ethyl acetate (1 x) and the combined organic layers were dried (Na2SO4) and evaporated under reduced pressure to give a yellow oil, which was purified by silica-gel chromatography (1:1 Pentane:EtOAc as eluant) to give the title compound as a colourless oil (0.499 g, 99%)

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customthe reaction mixture was evaporated under reduced pressure
  2. customthe residue partitioned between ethyl acetate and water
  3. extractionThe aqueous layer was then extracted with ethyl acetate (1 x)
  4. dry with materialthe combined organic layers were dried (Na2SO4)
  5. customevaporated under reduced pressure
  6. customto give a yellow oil, which
  7. customwas purified by silica-gel chromatography (1:1 Pentane:EtOAc as eluant)

出典と根拠

ORDレコード
ord-5640b55abd2342b98d780d8ad7459911
出典データセット
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05708174

反応ノート

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