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(5-Fluoro-6-methoxypyridin-3-yl)methanol → 5-Fluoro-6-methoxypyridine-3-carbaldehyde

HRID 1510684
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HRID 1510684 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH2:10][OH:11])[CH:5]=[N:6][C:7]=1[O:8][CH3:9]>ClCCl.[O-2].[O-2].[Mn+4]>[F:1][C:2]1[C:7]([O:8][CH3:9])=[N:6][CH:5]=[C:4]([CH:3]=1)[CH:10]=[O:11]
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참가 물질

4

반응물 1

HCID 57815441(5-Fluoro-6-methoxypyridin-3-yl)methanol

생성물 1

HCID 447547845-Fluoro-6-methoxypyridine-3-carbaldehyde수율 90%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매3회HCID 6344Dichloromethane용매3회

실험 절차

To a solution of 0.54 g of (5-fluoro-6-methoxypyridin-3-yl)methanol in 5 mL of dichloromethane, 1.5 g of manganese dioxide was added. The mixture was stirred at room temperature for 3 hours, thereto were then added 0.89 g of manganese dioxide and 4 mL of dichloromethane, and the mixture was stirred for 1 hour. Thereto were further added 1.5 g of manganese dioxide and 2 mL of dichloromethane, and the mixture was stirred at room temperature for 2 hours 30 minutes. After leaving overnight, the insoluble substance was filtered off, and the filtration residue was washed with chloroform. The solvent was distilled off under reduced pressure to obtain 0.48 g of 5-fluoro-6-methoxynicotinaldehyde as a yellow solid.

후처리

  1. stirringthe mixture was stirred for 1 hour
  2. stirringthe mixture was stirred at room temperature for 2 hours 30 minutes
  3. customAfter leaving overnight
  4. filtrationthe insoluble substance was filtered off
  5. washthe filtration residue was washed with chloroform
  6. distillationThe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-25887b04068c42b1beab8741d99a6679
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08211908B2

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