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(2-Chlorothiophen-3-yl)naphthalen-2-yl Methanol → (2-Chlorothiophen-3-yl)-(naphthalen-2-yl)-methanone

HRID 34010
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인쇄 미리보기

반응식

HRID 34010 반응식
[Cl:1][C:2]1[S:3][CH:4]=[CH:5][C:6]=1[CH:7]([C:9]1[CH:18]=[CH:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=1)[OH:8]>C1(C)C=CC=CC=1.[O-2].[O-2].[Mn+4]>[Cl:1][C:2]1[S:3][CH:4]=[CH:5][C:6]=1[C:7]([C:9]1[CH:18]=[CH:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=1)=[O:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 23070162(2-Chlorothiophen-3-yl)naphthalen-2-yl Methanol

생성물 1

HCID 23070192(2-Chlorothiophen-3-yl)-(naphthalen-2-yl)-methanone수율 52.1%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 1140Toluene용매

반응 조건

온도
50 °C

실험 절차

To a solution of 1.18 g of (2-chlorothiophen-3-yl)-(naphthalen-2-yl)-methanol in 12 mL of toluene was added 1.12 g of activated manganese dioxide at room temperature, and after stirring at 50° C. for a day, manganese dioxide was filtered off through Celite. The solvent was distilled off, and the resultant crude product was purified and separated by silica gel column chromatography (ethyl acetate:n-hexane=1:50), to afford 0.61 g of the title compound as a colorless oil.

후처리

  1. filtrationmanganese dioxide was filtered off through Celite
  2. distillationThe solvent was distilled off
  3. customthe resultant crude product was purified
  4. customseparated by silica gel column chromatography (ethyl acetate:n-hexane=1:50)

출처 및 근거

ORD 기록
ord-853adcebad0e4c17ad3678e7816250a7
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07429609B2

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