Ethanol → 4-Cyclopropyl-2-fluoroaniline

HRID 521823

반응식

HRID 521823 반응식
[CH:1]1([C:4]2[CH:9]=[CH:8][C:7]([N+:10]([O-])=O)=[C:6]([F:13])[CH:5]=2)[CH2:3][CH2:2]1.[Cl-].[NH4+].CCO.C1COCC1>O.[Fe]>[CH:1]1([C:4]2[CH:9]=[CH:8][C:7]([NH2:10])=[C:6]([F:13])[CH:5]=2)[CH2:3][CH2:2]1

참가 물질

7

실험 절차

A mixture of 4-cyclopropyl-2-fluoro-1-nitrobenzene (3.36 g, 18.55 mmol), powdered iron (4.35 g, 77.9 mmol), and 2M ammonium chloride in water (19.8 mL) and 3:2:1 v/v EtOH:THF:H2O (86 mL) was stirred at reflux under N2 for 17 h. The reaction mixture was cooled to RT and filtered through a pad of Celite. The Celite pad was rinsed well with ethyl acetate (˜50 mL). Saturated aqueous NaHCO3 solution was slowly added to the filtrate to neutralize the reaction mixture. The reaction mixture was extracted with ethyl acetate (3×200 mL). The combined organic layers were washed with water and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude residue was purified via flash column chromatography eluted with 0 to 75% ethyl acetate/hexane to give 2.80 g (99%) of an orange oil, which solidified at 20° C. 1H NMR (400 MHz, CDCl3) δ 6.75-6.63 (m, 3H), 3.57 (s, 2H), 1.87-1.72 (m, 1H), 0.93-0.83 (m, 2H), 0.64-0.51 (m, 2H); MS (ESI) m/z: 152.3 [M+H]+.

후처리

  1. temperatureat reflux under N2 for 17 h
  2. filtrationfiltered through a pad of Celite
  3. washThe Celite pad was rinsed well with ethyl acetate (˜50 mL)
  4. additionSaturated aqueous NaHCO3 solution was slowly added to the filtrate
  5. extractionThe reaction mixture was extracted with ethyl acetate (3×200 mL)
  6. washThe combined organic layers were washed with water and brine
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customThe crude residue was purified via flash column chromatography
  11. washeluted with 0 to 75% ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-9cf61468e3144c8db3cd7bd166c5a8c9
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09328106B2

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