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2-Octyl-1-benzofuran → 2-Octylcoumaran

HRID 3062
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인쇄 미리보기

반응식

HRID 3062 반응식
[CH2:1]([C:9]1[O:10][C:11]2[CH:17]=[CH:16][CH:15]=[CH:14][C:12]=2[CH:13]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]>C(O)C.[C].[Pd]>[CH2:1]([CH:9]1[CH2:13][C:12]2[C:11](=[CH:17][CH:16]=[CH:15][CH:14]=2)[O:10]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 37871882-Octyl-1-benzofuran

생성물 1

HCID 189343122-Octylcoumaran수율 94.6%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 702Ethanol용매

실험 절차

Then, 44 g of 2-octylbenzofuran was dissolved in 440 ml of ethanol. To the solution 35 g of 10%-palladium-carbon was added to effect catalytic reduction for 3 hours sunder normal pressure. After the reaction, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to obtain a residue. The residue was purified by silica gel column chromatography (eluent:hexane) to obtain 42 g of liquid 2-octylcoumaran (Yield: 94.6%).

후처리

  1. customfor 3 hours
  2. customAfter the reaction
  3. customthe catalyst was removed by filtration
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. customto obtain a residue
  6. customThe residue was purified by silica gel column chromatography (eluent:hexane)

출처 및 근거

ORD 기록
ord-f28ffd070d2241e988f52b5c36d20b5d
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05733476

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