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(3,5-Diethoxy-4-fluorophenyl)methanol → 3,5-Diethoxy-4-fluoro-benzaldehyde

HRID 547933
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HRID 547933 반응식
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([CH2:14][OH:15])[CH:7]=[C:8]([O:11][CH2:12][CH3:13])[C:9]=1[F:10])[CH3:2]>ClCCCl.O=[Mn]=O>[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([CH:7]=[C:8]([O:11][CH2:12][CH3:13])[C:9]=1[F:10])[CH:14]=[O:15])[CH3:2]
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참가 물질

4

반응물 1

HCID 59863043(3,5-Diethoxy-4-fluorophenyl)methanol

생성물 1

HCID 591282733,5-Diethoxy-4-fluoro-benzaldehyde

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 111,2-Dichloroethane용매

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온도
50 °C

실험 절차

To a solution of (3,5-diethoxy-4-fluoro-phenyl)-methanol (2.30 g, 10.7 mmol, 1.0 equiv) in 1,2-dichloroethane (50 mL) was added activated MnO2 (2.89 g, 33.3 mmol, 3.1 equiv). The reaction mixture was stirred for 21 h at 50° C. and then filtered through Hyflo Super Cel providing after evaporation of the solvent under reduced pressure 1.90 g (83%) of the title compound. 1H NMR (400 MHz, CDCl3): δ 1.38 (t, J=7.0 Hz, 6H), 4.09 (q, J=7.0 Hz, 4H), 7.04 (d, J=7.2 Hz, 2H), 9.75 (s, 1H). MS (EI): 212.1 [M]+.

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후처리

  1. filtrationfiltered through Hyflo Super Cel
  2. customproviding
  3. customafter evaporation of the solvent under reduced pressure 1.90 g (83%) of the title compound

출처 및 근거

ORD 기록
ord-7bcfb09e2441454991aba459a38637ba
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07939661B2

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