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Hydrogen Peroxide → 2,3-Epoxy-4-octyl-4-trimethylsilyloxycyclopentanone

HRID 1587131
ノート
印刷プレビュー

反応式

HRID 1587131 の反応式
[CH2:1]([C:9]1([O:15][Si:16]([CH3:19])([CH3:18])[CH3:17])[CH2:13][C:12](=[O:14])[CH:11]=[CH:10]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[OH:20]O.[OH-].[Na+].[Cl-].[NH4+]>CO>[O:14]1[CH:13]2[CH:12]1[C:11](=[O:20])[CH2:10][C:9]2([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[O:15][Si:16]([CH3:19])([CH3:18])[CH3:17]
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 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 25517Ammonium ChlorideHCID 137677604-Octyl-4-trimethylsilyloxy-2-cyclopentenone

生成物 1

HCID 197605912,3-Epoxy-4-octyl-4-trimethylsilyloxycyclopentanone

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 3.3 g of 4-octyl-4-trimethylsilyloxy-2-cyclopentenone dissolved in 50 ml of methanol was added, under ice-cooling and stirring, 5.0 ml of an aqueous 30% hydrogen peroxide, and 500 μl of an aqueous 1N sodium hydroxide was added. After the mixture was stirred for 3.5 hours, saturated aqueous ammonium chloride was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. The product was filtered and concentrated to give a crude oil of 2,3-epoxy-4-octyl-4-trimethylsilyloxycyclopentanone.

後処理

  1. additionwas added, under ice-
  2. temperaturecooling
  3. stirringAfter the mixture was stirred for 3.5 hours
  4. extractionthe mixture was extracted with ethyl acetate
  5. washThe organic layer was washed with saturated aqueous sodium chloride
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationThe product was filtered
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-096f1f93eb7945a78001cf724db05b2c
出典データセット
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05216183

反応ノート

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