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Hydrogen Peroxide → 2-(1-Hydroxycyclopentyl)acetic acid

HRID 1586907
ノート
印刷プレビュー

反応式

HRID 1586907 の反応式
[C@H:1]12[CH2:7][CH:4](CC1)[CH2:3][C:2]2=[O:8].[C:9]([O-:12])(=[O:11])[CH3:10].[Na+].OO>C(O)(=O)C>[OH:8][C:2]1([CH2:10][C:9]([OH:12])=[O:11])[CH2:3][CH2:4][CH2:7][CH2:1]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 784Hydrogen PeroxideHCID 517045Sodium AcetateHCID 54006847(1R)-Bicyclo(2.2.1)heptan-2-one

生成物 1

HCID 3482662-(1-Hydroxycyclopentyl)acetic acid収率 67%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

This product is oxidized by the Baeyer-Villiger procedure. (1R)-Norbornanone (81, 18 mmol) is stirred with sodium acetate (9 g, water-free), hydrogen peroxide (27 ml, 30%), and acetic acid (9 ml) at 5° C. in the dark for 40 hours. The reaction is quenched by the addition of sodium sulfite (50 ml of a 10% aqueous solution) at 0° C. The product is extracted twice with EtOAc (600 ml). The extract is washed with the sodium sulfite solution, then with sodium bicarbonate solution (50 ml, saturated), then with sodium chloride solution (saturated), dried and evaporated. The product is chromatographed on silica (380 g, ether) to yield the lacton of 3 hydroxycyclopentane-1-acetic acid (82, 12 mmol, 67%).

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 is quenched by the addition of sodium sulfite (50 ml of a 10% aqueous solution) at 0° C
  2. extractionThe product is extracted twice with EtOAc (600 ml)
  3. washThe extract is washed with the sodium sulfite solution
  4. dry with materialwith sodium bicarbonate solution (50 ml, saturated), then with sodium chloride solution (saturated), dried
  5. customevaporated
  6. customThe product is chromatographed on silica (380 g, ether)

出典と根拠

ORDレコード
ord-7c2649edde5f475783fa29eb77f4d231
出典データセット
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05216141

反応ノート

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