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p-Fluoronitrobenzene → HCID 7062386, 화합물

HRID 1713808
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HRID 1713808 반응식
F[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][CH:3]=1.[CH3:11][C@H:12]1[O:17][C@@H:16]([CH3:18])[CH2:15][NH:14][CH2:13]1.C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[CH3:18][C@H:16]1[O:17][C@@H:12]([CH3:11])[CH2:13][N:14]([C:2]2[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][CH:3]=2)[CH2:15]1
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참가 물질

5

반응물 3

HCID 9590p-FluoronitrobenzeneHCID 11430Potassium CarbonateHCID 6415002,6-Dimethylmorpholine, cis-

생성물 1

HCID 7062386HCID 7062386, 화합물수율 99%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

1-Fluoro-4-nitrobenzene (4.9 g, 34.75 mmol) was added to a stirred mixture of cis-2,6-dimethylmorpholine (44.4 g, 38.26 mmol) and anhydrous potassium carbonate (2.5 g, 18.12 mmol) in acetonitrile (50 mL). The mixture was heated under reflux for 19 h, cooled, filtered and the solid washed with acetonitrile. The filtrate was concentrated by evaporation to give the title compound (8.1 g, 99%) as a solid; 1H NMR δ (CDCl3): 8.13 (2H, d), 6.82 (2H, d), 3.76 (2H, m), 3.66 (2H, dt), 2.61 (2H, t), 1.28 (6H, d); MS m/e MH+: 237.

후처리

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 19 h
  3. temperaturecooled
  4. filtrationfiltered
  5. washthe solid washed with acetonitrile
  6. concentrationThe filtrate was concentrated by evaporation

출처 및 근거

ORD 기록
ord-a46cf8cfed1844fcb4039d4757171f49
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07795283B2

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