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Benzhydrol → p-Menth-1-ene oxide

HRID 1976869
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HRID 1976869 반응식
[C:1]1([CH3:10])[CH2:6][CH2:5][CH:4]([CH:7]([CH3:9])[CH3:8])[CH2:3][CH:2]=1.C([OH:24])(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>[C:1]12([CH3:10])[O:24][CH:2]1[CH2:3][CH:4]([CH:7]([CH3:9])[CH3:8])[CH2:5][CH2:6]2
참가 물질반응 조건실험 절차출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 7037BenzhydrolHCID 7368(Trifluoromethyl)benzeneHCID 10665N-HydroxyphthalimideHCID 21671p-Menth-1-ene2회HCID 36719Hexafluoroacetone trihydrate

생성물 1

HCID 524011p-Menth-1-ene oxide수율 42%

시약·촉매·용매 1

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

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온도
60 °C

실험 절차

A mixture of 3mmol of 1-p-menthene, 15mmol of benzhydrol, 0.3 mmol of N-hydroxyphthalimide, 0.0015 mmol of cobalt (II) acetate, 0.3 mmol of hexafluoroacetone trihydrate, and 3 ml of trifluoromethylbenzene was stirred at 60° C. under an oxygen atmosphere (1 atm) for 12 hours. Gas chromatographic analysis of products in a reaction mixture revealed that 1-p-menthene was converted, at a rate of 63%, into 1-p-menthene oxide (yield: 42%).

출처 및 근거

ORD 기록
ord-7e136347c7ac4d679d9651a9b3beb389
출처 데이터셋
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06229023B1

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