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(E)-5-[4-(Trifluoromethyl)phenyl]-2-penten-4-yn-1-ol → (E)-5-(4-(Trifluoromethyl)phenyl]-2-penten-4-ynal

HRID 379956
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인쇄 미리보기

반응식

HRID 379956 반응식
[F:1][C:2]([F:16])([F:15])[C:3]1[CH:8]=[CH:7][C:6]([C:9]#[C:10]/[CH:11]=[CH:12]/[CH2:13][OH:14])=[CH:5][CH:4]=1>C(Cl)Cl.[O-2].[O-2].[Mn+4]>[F:1][C:2]([F:15])([F:16])[C:3]1[CH:4]=[CH:5][C:6]([C:9]#[C:10]/[CH:11]=[CH:12]/[CH:13]=[O:14])=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 18363296(E)-5-[4-(Trifluoromethyl)phenyl]-2-penten-4-yn-1-ol

생성물 1

HCID 18363293(E)-5-(4-(Trifluoromethyl)phenyl]-2-penten-4-ynal수율 70.1%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 6344Dichloromethane용매

실험 절차

In 4 ml of methylene chloride were dissolved 350 mg (1.56 mmol) of (E)-5-[4-(trifluoromethyl)phenyl]-2-penten-4-yn-1-ol, and 3.5 g of active manganese dioxide were added to the solution, followed by stirring of the resulting mixture at room temperature for 30 minutes. The solid was removed by filtration and the filtrate was concentrated. Then, the filtrate was subjected to column chromatography using 10 g of silica gel and eluted with a mixed solvent of ethyl acetate-hexane (1:24) to obtain 245 mg (yield: 70%) of the title compound as an oil.

후처리

  1. additionwere added to the solution
  2. customThe solid was removed by filtration
  3. concentrationthe filtrate was concentrated
  4. washeluted with a mixed solvent of ethyl acetate-hexane (1:24)

출처 및 근거

ORD 기록
ord-9920da54fb77480c9c10d9e1b93d7a8c
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06300357B1

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