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

HRID 1587131
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HRID 1587131 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 25517Ammonium ChlorideHCID 137677604-Octyl-4-trimethylsilyloxy-2-cyclopentenone

생성물 1

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

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-096f1f93eb7945a78001cf724db05b2c
출처 데이터셋
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05216183

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