Methylamine → Methyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)amine

HRID 1168949Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1168949
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[C:8]([O:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:9]=[N:10][CH:11]=1.[CH3:20][NH2:21]>CO>[CH3:20][NH:21][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[N:10][CH:9]=[C:8]([O:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:7]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

The 5-(3-chloropropoxy)-3-(phenylmethoxy)pyridine (1.52 g, 5.49 mmol) was dissolved in methanol (25 mL) and added to a 40 wt % aqueous solution of methylamine (50 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 4 h. After cooling, the mixture was concentrated by rotary evaporation. Saturated NaCl solution (25 mL) was added to the residue. The pH of the solution was adjusted to 6, and impurities were extracted with ether (3×15 mL). The aqueous layer was basified to pH 10 with 10% NaOH solution and extracted with chloroform (4×15 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 1.07 g (71.7%) of an oil.

Aufarbeitung

  1. customThe tube was sealed
  2. temperatureAfter cooling
  3. concentrationthe mixture was concentrated by rotary evaporation
  4. additionSaturated NaCl solution (25 mL) was added to the residue
  5. extractionwere extracted with ether (3×15 mL)
  6. extractionextracted with chloroform (4×15 mL)
  7. dry with materialThe combined chloroform extracts were dried (Na2SO4)
  8. filtrationfiltered
  9. concentrationconcentrated by rotary evaporation to a residue that
  10. customwas dried briefly under high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-3f8d37cf7c974bdf8e7c5cf9d164df54
Quelldatensatz
uspto-grants-2003_09
Patentnummer
US06627648B1

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