Ammonium Hydroxide → 3-(2-Aminoethoxy)pyridine

HRID 1168910노트

반응식

HRID 1168910 반응식
Cl[CH2:2][CH2:3][O:4][C:5]1[CH:6]=[N:7][CH:8]=[CH:9][CH:10]=1.[OH-].[NH4+:12]>CO>[N:7]1[CH:8]=[CH:9][CH:10]=[C:5]([O:4][CH2:3][CH2:2][NH2:12])[CH:6]=1

참가 물질

4

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온도
125 °C

실험 절차

The 2-chloro-1-(3-pyridyloxy)ethane (1.23 g, 7.80 mmol) was dissolved in methanol (25 mL) and added to concentrated ammonium hydroxide solution (29.7%, 14.8 M, 55 mL) in a heavy-walled glass pressure-tube apparatus. The tube was sealed and the mixture was stirred and heated at 125° C. (oil bath temperature) for 42 h. After cooling, the mixture was concentrated by rotary evaporation. Saturated NaCl solution (10 mL) was added to the residue, and the solution (pH 6) was extracted with ether (3×25 mL) to remove impurities. The aqueous layer was diluted with saturated NaCl solution (15 mL) and basified to pH 12 with 10% NaOH solution (5 mL). The mixture was extracted with chloroform (4×50 mL). The combined light-yellow chloroform extracts were dried (Na2SO4), filtered, and concentrated by rotary evaporation to a residue that was dried briefly under high vacuum to give 0.390 g (36.2%) of a light-yellow oil.

후처리

  1. customThe tube was sealed
  2. temperatureAfter cooling
  3. concentrationthe mixture was concentrated by rotary evaporation
  4. additionSaturated NaCl solution (10 mL) was added to the residue
  5. extractionthe solution (pH 6) was extracted with ether (3×25 mL)
  6. customto remove impurities
  7. additionThe aqueous layer was diluted with saturated NaCl solution (15 mL)
  8. extractionThe mixture was extracted with chloroform (4×50 mL)
  9. dry with materialThe combined light-yellow chloroform extracts were dried (Na2SO4)
  10. filtrationfiltered
  11. concentrationconcentrated by rotary evaporation to a residue that
  12. customwas dried briefly under high vacuum

출처 및 근거

ORD 기록
ord-eb3d74b1be01492cb0f8ecaa5adab776
출처 데이터셋
uspto-grants-2003_09
특허 번호
US06627648B1

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