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2-Fluoroaniline → 2-Fluoro-n-(2-nitrophenyl)aniline

HRID 1818769
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HRID 1818769 반응식
[F:1][C:2]1[CH:8]=[CH:7][CH:6]=[CH:5][C:3]=1[NH2:4].[H-].[Na+].F[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[N+:18]([O-:20])=[O:19]>CN(C=O)C>[F:1][C:2]1[CH:8]=[CH:7][CH:6]=[CH:5][C:3]=1[NH:4][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[N+:18]([O-:20])=[O:19]
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참가 물질

5

반응물 3

HCID 95842-FluoroanilineHCID 24758Sodium hydrideHCID 738951-Fluoro-2-nitrobenzene

생성물 1

HCID 2613812-Fluoro-n-(2-nitrophenyl)aniline수율 60.3%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

2-Fluoroaniline (1.45 mL, 15 mmol) was dissolved in DMF (10 mL) and sodium hydride (0.58 g, 15 mmol) was added and the mixture was stirred for 30 minutes. 2-Fluoronitrobenzene (1.05 mL, 10 mmol) was added and the mixture was stirred for 16 hours. The mixture was quenched with saturated NH4Cl and diluted with ether. The mixture was washed with water, brine, dried over anhydrous magnesium sulfate, and concentrated. The crude product was purified via Isco chromatography (Redisep, silica, gradient 5-30% ethyl acetate in hexane) to afford 1.4 g 2-fluoro-N-(2-nitrophenyl)aniline that was carried on directly to the next step. MS (ES) m/z 232.9.

후처리

  1. stirringthe mixture was stirred for 16 hours
  2. customThe mixture was quenched with saturated NH4Cl
  3. additiondiluted with ether
  4. washThe mixture was washed with water, brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated
  7. customThe crude product was purified via Isco chromatography (Redisep, silica, gradient 5-30% ethyl acetate in hexane)

출처 및 근거

ORD 기록
ord-e2586e9d43c84e8888da876a19761053
출처 데이터셋
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07601722B2

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