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Hydrogen Peroxide → 20-(5,5-Dimethyl-1,3-dioxan-2-yl)-1alpha,2alpha-epoxypregna-4,6-dien-3-one

HRID 1196313
ノート
印刷プレビュー

反応式

HRID 1196313 の反応式
[OH-].[Na+].OO.[CH3:5][C:6]1([CH3:34])[CH2:11][O:10][CH:9]([CH:12]([C@@H:14]2[C@:31]3([CH3:32])[C@H:17]([C@H:18]4[C@H:28]([CH2:29][CH2:30]3)[C@:26]3([CH3:27])[C:21](=[CH:22][C:23](=[O:33])[CH:24]=[CH:25]3)[CH:20]=[CH:19]4)[CH2:16][CH2:15]2)[CH3:13])[O:8][CH2:7]1.C(OCC)(=[O:37])C.CCCCCC>CO.O>[CH3:34][C:6]1([CH3:5])[CH2:7][O:8][CH:9]([CH:12]([C@@H:14]2[C@:31]3([CH3:32])[C@H:17]([C@H:18]4[C@H:28]([CH2:29][CH2:30]3)[C@:26]3([CH3:27])[C:21](=[CH:22][C:23](=[O:33])[C@@H:24]5[O:37][C@@H:25]53)[CH:20]=[CH:19]4)[CH2:16][CH2:15]2)[CH3:13])[O:10][CH2:11]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 21226206Ethyl acetate hexaneHCID 2284393220-(5,5-Dimethyl-1,3-dioxan-2-yl)pregna-1,4,6-trien-3-one

生成物 1

HCID 8674579720-(5,5-Dimethyl-1,3-dioxan-2-yl)-1alpha,2alpha-epoxypregna-4,6-dien-3-one収率 77%

試薬・触媒・溶媒 2

HCID 887
Methanol
溶媒
2 回
HCID 962Water溶媒2 回

実験手順

A 10 weight % solution of sodium hydroxide in methanol (1.16 ml) and 6.36 ml of a 30 weight % solution of hydrogen peroxide in water (containing 62.3 mmoles of hydrogen peroxide) were added to a solution of 4.66 g (11.3 mmoles) of 20-(5,5-dimethyl-1,3-dioxan-2-yl)pregna-1,4,6-trien-3-one in 150 ml of methanol and the mixture was stirred at room temperature for 16 hours. The reaction mixture thus obtained was diluted with water and after the methanol was partially distilled off under reduced pressure at room temperature, the residue was extracted with ether. The extract was washed successively with aqueous potassium iodide solution and aqueous sodium chloride solution and the organic layer was dried over magnesium sulfate. The solvent was then distilled off under reduced pressure and the residue was purified by silica gel chromatography (eluent: ethyl acetate/hexane=1:10, v/v) to recover 3.72 g of 20-(5,5-dimethyl-1,3-dioxan-2-yl)-1α,2α-epoxypregna-4,6-dien-3-one (yield: 77%).

後処理

  1. customThe reaction mixture thus obtained
  2. distillationafter the methanol was partially distilled off under reduced pressure at room temperature
  3. extractionthe residue was extracted with ether
  4. washThe extract was washed successively with aqueous potassium iodide solution and aqueous sodium chloride solution
  5. dry with materialthe organic layer was dried over magnesium sulfate
  6. distillationThe solvent was then distilled off under reduced pressure
  7. customthe residue was purified by silica gel chromatography (eluent

出典と根拠

ORDレコード
ord-6d7909af6ace465cb48f8d3d6c5a4501
出典データセット
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05112998

反応ノート

読み込み中…

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