Methylamine → HCID 10176686, compound

HRID 2305733Notes

Reaction equation

HRID 2305733 reaction equation
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[CH:7]=1.[CH3:15][NH2:16]>CO>[CH3:15][NH:16][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[CH:7]=1

Participants

4

Conditions

Temperature
100 °C

Procedure

The 1-(3-chloropropoxy)-3-nitrobenzene (1.00 g, 4.65 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 493 mg (50.6%) of an oil.

Workup

  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

Sources & evidence

ORD record
ord-dae9ccb19d7145a3b2e78cda0dc29417
Source dataset
uspto-grants-2002_08
Patent number
US06441006B2

Reaction notes

Loading…