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Potassium Carbonate → 1-(2-Fluoro-4-nitrophenyl)pyrrolidin-3-ol

HRID 1418664
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HRID 1418664 반응식
[NH:1]1[CH2:5][CH2:4][CH:3]([OH:6])[CH2:2]1.[F:7][C:8]1[CH:9]=[C:10]([N+:15]([O-:17])=[O:16])[CH:11]=[CH:12][C:13]=1F.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[F:7][C:8]1[CH:9]=[C:10]([N+:15]([O-:17])=[O:16])[CH:11]=[CH:12][C:13]=1[N:1]1[CH2:5][CH2:4][CH:3]([OH:6])[CH2:2]1
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참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 982104-HydroxypyrrolidineHCID 1230531,2-Difluoro-4-nitrobenzene

생성물 1

HCID 219165861-(2-Fluoro-4-nitrophenyl)pyrrolidin-3-ol수율 113.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 3-pyrrolidinol (1.82 g) and 3,4-difluoronitrobenzene (3.0 g) in dimethylformamide (30 ml) was added potassium carbonate (3.94 g). The mixture was stirred at room temperature overnight and then filtered followed by washing with dichloromethane. The filtrate combined was concentrated under reduced pressure. The residue obtained was chromatographed over a silica gel column eluting with ethyl acetate/hexane with increasing in the content of ethyl acetate (50% to 60%). The appropriate fractions were pooled and concentrated under reduced pressure to give the title compound (4.83 g); 1H NMR (CD3OD, 270 MHz), δ 0.85 (2H, m), 2.25-2.57 (4H, m), 3.26 (1H, m), 5.47 (1H, t, J=8.6 Hz), 6.62 (1H, dd, J=2.4, 14.0 Hz), 6.69 (1H, dd, J=2.4, 8.6 Hz).

후처리

  1. filtrationfiltered
  2. washby washing with dichloromethane
  3. concentrationThe filtrate combined was concentrated under reduced pressure
  4. customThe residue obtained
  5. customwas chromatographed over a silica gel column
  6. washeluting with ethyl acetate/hexane
  7. temperaturewith increasing in the content of ethyl acetate (50% to 60%)
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-2847fd54f4824f13a990ba246f036cb5
출처 데이터셋
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05883093

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