Methylamine → HCID 10219684, compound

HRID 2305720Notes

Reaction equation

HRID 2305720 reaction equation
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[C:7]([CH3:12])=[N:8][CH:9]=[CH:10][CH:11]=1.[CH3:13][NH2:14]>CO>[CH3:13][NH:14][CH2:2][CH2:3][CH2:4][O:5][C:6]1[C:7]([CH3:12])=[N:8][CH:9]=[CH:10][CH:11]=1

Participants

4

Conditions

Temperature
100 °C

Procedure

The 3-chloro-1-(2-methyl(3-pyridyloxy))propane (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 NaCI solution (25 mL) was added to the residue. The pH of the solution was adjusted to 6, and the mixture was extracted with ether (3×25 mL) to remove impurities. The aqueous layer was basified to pH 10 with 100% NaOH solution and extracted with chloroform (4×50 mL). The combined chloroform extracts were dried (Na2SO4), filtered, and concentrated to give 1.19 g (61.0%) of an oil.

Workup

  1. customThe tube was sealed
  2. temperatureAfter cooling
  3. concentrationthe mixture was concentrated by rotary evaporation
  4. additionSaturated NaCI solution (25 mL) was added to the residue
  5. extractionthe mixture was extracted with ether (3×25 mL)
  6. customto remove impurities
  7. extractionextracted with chloroform (4×50 mL)
  8. dry with materialThe combined chloroform extracts were dried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated

Sources & evidence

ORD record
ord-0d073d2d9b5a49efa1e6d7934f2af1b1
Source dataset
uspto-grants-2002_08
Patent number
US06441006B2

Reaction notes

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