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(2-Fluoro-5-(2-fluoropyridin-3-yl)phenyl)methanol → 2-Fluoro-5-(2-fluoropyridin-3-yl)benzaldehyde

HRID 335948
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HRID 335948 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([F:14])=[N:10][CH:11]=[CH:12][CH:13]=2)=[CH:4][C:3]=1[CH2:15][OH:16].[Cr](Cl)([O-])(=O)=O.[NH+]1C=CC=CC=1>ClCCl>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([F:14])=[N:10][CH:11]=[CH:12][CH:13]=2)=[CH:4][C:3]=1[CH:15]=[O:16]
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참가 물질

4

반응물 2

HCID 67383551(2-Fluoro-5-(2-fluoropyridin-3-yl)phenyl)methanolHCID 178418287HCID 178418287, 화합물

생성물 1

HCID 866584942-Fluoro-5-(2-fluoropyridin-3-yl)benzaldehyde수율 187.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

(2-Fluoro-5-(2-fluoropyridin-3-yl)phenyl)methanol (2.54 g) was dissolved in dichloromethane (200 mL). Silica gel (30 mL) was added followed by pyridinium chlorochromate (5.31 g, 24.63 mmol). It was stirred at RT and monitored by TLC. Once the oxidation was complete the mixture was filtered through a pad of silica gel (10 mL) and washed with ethyl acetate. Evaporation under reduced pressure gave the desired 2-fluoro-5-(2-fluoropyridin-3-yl)benzaldehyde (4.71 g, 21.49 mmol, 87% yield) as an off white solid. MS m/z=220.1 [M+H]+. Calculated for C12H7F2NO: 219.05.

후처리

  1. additionSilica gel (30 mL) was added
  2. filtrationwas filtered through a pad of silica gel (10 mL)
  3. washwashed with ethyl acetate
  4. customEvaporation under reduced pressure

출처 및 근거

ORD 기록
ord-9151dffb4b1d4ca7bd12ae9340916a2d
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08883782B2

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