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Ethanol → 5-Ethoxy-2-nitroaniline

HRID 272717
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HRID 272717 반응식
[Na].Cl[C:3]1[CH:4]=[CH:5][C:6]([N+:10]([O-:12])=[O:11])=[C:7]([CH:9]=1)[NH2:8].[CH2:13]([OH:15])[CH3:14]>>[CH2:13]([O:15][C:3]1[CH:4]=[CH:5][C:6]([N+:10]([O-:12])=[O:11])=[C:7]([CH:9]=1)[NH2:8])[CH3:14]
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참가 물질

4

반응물 3

HCID 702EthanolHCID 742185-Chloro-2-nitroanilineHCID 5360545Sodium2회

생성물 1

HCID 51417895-Ethoxy-2-nitroaniline수율 94%

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온도
80 °C

실험 절차

A mixture of sodium metal (1.86 g, 80.9 mmol) and ethanol (65 mL) was stirred at ambient temperature until all of the sodium metal had been consumed. 5-Chloro-2-nitroaniline (4.64 g, 26.9 mmol) was added and the mixture was heated at 80° C. for 48 hours, cooled to room temperature, quenched with water, concentrated under vacuum, diluted with ethyl acetate, washed with water and brine, dried (MgSO4), filtered, and concentrated under vacuum. The residue was purified by column chromatography on silica gel with 7:3 hexane/ethyl acetate to provide 4.6 g (94%) of the desired product. MS (ESI) m/e 183 (M+H)+; 1H NMR (300 MHz, DMSO-d6) □ 7.90 (d, J=9.5 Hz, 1H), 7.46 (br s, 2H), 6.43 (d, J=2.7 Hz, 1H), 6.23 (dd, J=2.7, 9.5 Hz, 1H), 4.04 (q, J=7.1 Hz, 2H), 1.33 (t, J=7.0 Hz, 3H).

후처리

  1. customhad been consumed
  2. temperaturecooled to room temperature
  3. customquenched with water
  4. concentrationconcentrated under vacuum
  5. additiondiluted with ethyl acetate
  6. washwashed with water and brine
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationconcentrated under vacuum
  10. customThe residue was purified by column chromatography on silica gel with 7:3 hexane/ethyl acetate

출처 및 근거

ORD 기록
ord-69d3a98b3e5440f0b5e0634bc21a6715
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07456169B2

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