Ammonium Hydroxide → 3-(3-Pyridyloxy)propylamine

HRID 2305695노트

반응식

HRID 2305695 반응식
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1.[OH-].[NH4+:13]>CO>[N:8]1[CH:9]=[CH:10][CH:11]=[C:6]([O:5][CH2:4][CH2:3][CH2:2][NH2:13])[CH:7]=1

참가 물질

4

반응 조건

온도
100 °C

실험 절차

The 3-chloro-1-(3-pyridyloxy)propane (1.98 g, 11.6 mmol) was dissolved in methanol (25 mL) and added to concentrated ammonium hydroxide solution (29.70% 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 100° C. (oil bath temperature) for 6 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 basified to pH 10 with 100% NaOH solution, and the mixture was extracted with chloroform (4×25 mL). The combined chloroform extracts were dried (Na2SO4), filtered, and concentrated by rotary evaporation to a residue that was dried briefly under high vacuum to give 0.354 g (20.1%) of an 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. extractionthe mixture was extracted with chloroform (4×25 mL)
  8. dry with materialThe combined chloroform extracts were dried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated by rotary evaporation to a residue that
  11. customwas dried briefly under high vacuum

출처 및 근거

ORD 기록
ord-01c505bfd33242728ea41f7d13856192
출처 데이터셋
uspto-grants-2002_08
특허 번호
US06441006B2

반응 노트

불러오는 중…