Iodoethane → 2-Fluoro-4-ethylthioaniline

HRID 1793043노트

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HRID 1793043 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]#N)=[CH:4][C:3]=1[F:11].[CH2:12](I)C>C(O)C.O>[F:11][C:3]1[CH:4]=[C:5]([S:8][CH2:9][CH3:12])[CH:6]=[CH:7][C:2]=1[NH2:1]

참가 물질

5

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온도
50 °C

실험 절차

A solution of the product of Example 26, Step A, 4-amino-3-fluorophenyl thiocyanate (500 mg, 2.97 mmol), in ethanol (7 mL) was added dropwise to a solution of Na2S.9H2O (714 mg, 2.97 mmol) in water (1.5 mL) and the resulting mixture stirred at 50° C. for 1 hour. A solution of ethyl iodide (510 mg, 3.27 mmol) in ethanol (1 mL) was then added and the reaction stirred at 50° C. for a further 6 hours. The mixture was diluted with water (30 mL) and extracted with Et2O (4×10 mL), then the combined Et2O extracts washed with water (3×20 mL), saturated NaCl (20 mL) and dried (Na2SO4). Removal of the solvent under reduced pressure afforded a pale yellow oil which was purified by dry flash column chromatography on silica (5% Et2O/hexanes as eluant) to afford 2-fluoro-4-ethylthioaniline as a colourless oil (470 mg, 92%). 1H NMR (400 MHz, CDCl3) δ 7.08 (dd, J=11.3, 2.0 Hz, 1 H), 7.01 (ddd, J=8.2, 2.0, 0.9 Hz, 1 H), 6.71 (dd, J=9.3, 8.2 Hz, 1 H), 3.81 (br s, 2 H), 2.80 (q, J=7.3 Hz, 2 H), 1.24 (t, J=7.3 Hz, 3 H).

후처리

  1. stirringthe reaction stirred at 50° C. for a further 6 hours
  2. extractionextracted with Et2O (4×10 mL)
  3. washthe combined Et2O extracts washed with water (3×20 mL), saturated NaCl (20 mL)
  4. dry with materialdried (Na2SO4)
  5. customRemoval of the solvent under reduced pressure
  6. customafforded a pale yellow oil which
  7. customwas purified
  8. customby dry flash column chromatography on silica (5% Et2O/hexanes as eluant)

출처 및 근거

ORD 기록
ord-0951191161c74f289d2fe6513a0f5e04
출처 데이터셋
uspto-grants-2006_07
특허 번호
US07078438B2

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