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Benzhydrol → 1,2-Epoxy-3-octanol

HRID 1976868
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인쇄 미리보기

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HRID 1976868 반응식
[CH2:1]=[CH:2][CH:3]([OH:9])[CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].C([OH:23])(C1C=CC=CC=1)C1C=CC=CC=1.ON1C(=O)C2=CC=CC=C2C1=O.O.O.O.FC(F)(F)C(C(F)(F)F)=O.FC(C1C=CC=CC=1)(F)F>C([O-])(=O)C.[Co+2].C([O-])(=O)C>[O:23]1[CH:2]([CH:3]([OH:9])[CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[CH2:1]1
참가 물질반응 조건실험 절차출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 7037BenzhydrolHCID 7368(Trifluoromethyl)benzeneHCID 10665N-HydroxyphthalimideHCID 188271-Octen-3-Ol2회HCID 36719Hexafluoroacetone trihydrate

생성물 1

HCID 102908541,2-Epoxy-3-octanol수율 40%

시약·촉매·용매 1

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온도
60 °C

실험 절차

A mixture of 3mmol of 1-octen-3-ol, 15mmol of benzhydrol, 0.3 mmol of N-hydroxyphthalimide, 0.0015 mmol of cobalt (II) acetate, 0.6 mmol of hexafluoroacetone trihydrate, and 3 ml of trifluoromethylbenzene was stirred at 60° C. under an oxygen atmosphere (1 atm) for 24 hours. Gas chromatographic analysis of products in a reaction mixture revealed that 1-octen-3-ol was converted, at a rate of 43%, into 1,2-epoxy-3-octanol (yield: 40%).

출처 및 근거

ORD 기록
ord-b76c200635054022a293f89e44cb585f
출처 데이터셋
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06229023B1

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이 페이지에서참가 물질반응 조건실험 절차출처 및 근거반응 노트
HCID 6277
Cobalt diacetate
촉매