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Hydrogen Peroxide → 1,2-Epoxydecane

HRID 650280
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HRID 650280 반응식
[CH2:1]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].ClCCl.[OH:14]O>O.[O-2].[O-2].[Mn+4]>[CH2:1]1[O:14][CH:2]1[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 784Hydrogen PeroxideHCID 6344DichloromethaneHCID 133811-Decene

생성물 1

HCID 169931,2-Epoxydecane수율 94%

시약·촉매·용매 3

HCID 962Water촉매HCID 178418406HCID 178418406, 화합물촉매
HCID 962
Water
용매

실험 절차

In a 25 mL scintillation vial equipped with a magnetic stirrer, 1-decene (1.41 g, 10 mmol) was placed followed by addition of 4 mL dichloromethane. To this solution was added BTSP (2.8 g, 15 mmol). The vial was immersed into ice/water bath. After 5 minutes Re2O7 (24 mg, 0.05 mmol)5 was added followed by 10 μL of water. The reaction turned bright yellow and was allowed to warm up to room temperature and stirred for 14 h. Upon completion, water (3 drops) was added followed by manganese dioxide (ca. 5 mg) in order to decompose the remaining H2O2. The destruction of H2O2 was evident by the disappearance of yellow color. The mixture was then dried over Na2SO4. Concentration afforded 1-decene oxide (1.48 g, 94% yield) of a colorless oil.

후처리

  1. customIn a 25 mL scintillation vial equipped with a magnetic stirrer
  2. additionTo this solution was added BTSP (2.8 g, 15 mmol)
  3. customThe vial was immersed into ice/water bath
  4. customThe destruction of H2O2
  5. dry with materialThe mixture was then dried over Na2SO4
  6. concentrationConcentration

출처 및 근거

ORD 기록
ord-6a4c29db4f9847e09dddbc803b75e053
출처 데이터셋
uspto-grants-2001_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06271400B1

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