Methylamine → Methyl(4-(3-pyridyloxy)butyl)amine

HRID 2305701Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2305701
Cl[CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=1.[CH3:13][NH2:14]>CO>[CH3:13][NH:14][CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

The 4-chloro-1-(3-pyridyloxy)butane (2.00 g, 10.8 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 (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 1.47 g (75.5%) of an oil.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-6f66983fada8465f851f8fd911db6e01
Quelldatensatz
uspto-grants-2002_08
Patentnummer
US06441006B2

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