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4-Methoxyphenol → 3-Fluoro-4-(4-methoxy-phenoxy)-benzaldehyde

HRID 1406335
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인쇄 미리보기

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HRID 1406335 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([OH:9])=[CH:5][CH:4]=1.[F:10][C:11]1[CH:12]=[C:13]([CH:16]=[CH:17][C:18]=1F)[CH:14]=[O:15]>CC(N(C)C)=O>[F:10][C:11]1[CH:12]=[C:13]([CH:16]=[CH:17][C:18]=1[O:9][C:6]1[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1)[CH:14]=[O:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 90154-MethoxyphenolHCID 5880883,4-Difluorobenzaldehyde

생성물 1

HCID 286041023-Fluoro-4-(4-methoxy-phenoxy)-benzaldehyde

시약·촉매·용매 1

HCID 31374Dimethylacetamide용매

반응 조건

온도
110 °C

실험 절차

4.9 g (40 mmol) of 4-methoxy-phenol and 4.4 ml (40 mmol) of 3,4-difluorobenzaldehyde were dissolved in 40 ml DMA and stirred in a microwave (CEM Explorer) for 15 minutes at 110° C., then filtered through basic Alox, washed with DMF and concentrated by rotary evaporation. The residue was separated through a KG column with a gradient (cyclohexane+10-25% ethyl acetate) and concentrated by rotary evaporation.

후처리

  1. filtrationfiltered through basic Alox
  2. washwashed with DMF
  3. concentrationconcentrated by rotary evaporation
  4. customThe residue was separated through a KG column with a gradient (cyclohexane+10-25% ethyl acetate)
  5. concentrationconcentrated by rotary evaporation

출처 및 근거

ORD 기록
ord-6d694ab1a44541eebdc880fadf9c7f6a
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08916589B2

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