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5-(Hydroxymethyl)-1,3-Dihydro-2H-Indol-2-One → 2,3-Dihydro-2-oxo-1H-indole-5-carboxaldehyde

HRID 748527
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HRID 748527 반응식
[OH:1][CH2:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[O:12])[CH2:6]2>N1C=CC=CC=1.[O-2].[Cr+6].[O-2].[O-2]>[O:12]=[C:7]1[CH2:6][C:5]2[C:9](=[CH:10][CH:11]=[C:3]([CH:2]=[O:1])[CH:4]=2)[NH:8]1
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참가 물질

4

반응물 1

HCID 597510365-(Hydroxymethyl)-1,3-Dihydro-2H-Indol-2-One

생성물 1

HCID 597510372,3-Dihydro-2-oxo-1H-indole-5-carboxaldehyde수율 46.5%

시약·촉매·용매 2

HCID 10219390chromium (VI) trioxide촉매HCID 1049Pyridine용매3회

실험 절차

Chromium(VI) oxide (240 mg, 2.4 mmol) was added to ice-cooled pyridine (3 mL). To the formed yellow suspension was added additional pyridine (2 mL) and 5-(hydroxymethyl)-1,3-dihydro-2H-indol-2-one (130 mg, 0.8 mmol) dissolved in pyridine (3 mL). The reaction was quenched after 15 min by the addition of water (50 mL) and extracted with ethyl acetate. The organic phases were dried (Na2SO4) and evaporated in vacuo. The crude product was purified on a silica gel column using methylene chloride/methanol, (10:1), as the eluent to give 60 mg (46% yield) of the title compound.

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후처리

  1. customThe reaction was quenched after 15 min by the addition of water (50 mL)
  2. extractionextracted with ethyl acetate
  3. dry with materialThe organic phases were dried (Na2SO4)
  4. customevaporated in vacuo
  5. customThe crude product was purified on a silica gel column

출처 및 근거

ORD 기록
ord-73aaf4bb5c9b4022bdddf3a66a66430b
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07399780B2

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