Ammonium Hydroxide → 3-(3-Pyridyloxy)propylamine
Reaction equation
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]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
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 (29.7%, 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 10% 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.
Workup
- customThe tube was sealed
- temperatureAfter cooling
- concentrationthe mixture was concentrated by rotary evaporation
- additionSaturated NaCl solution (10 mL) was added to the residue
- extractionthe solution (pH 6) was extracted with ether (3×25 mL)
- customto remove impurities
- extractionthe mixture was extracted with chloroform (4×25 mL)
- dry with materialThe combined chloroform extracts were dried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated by rotary evaporation to a residue that
- customwas dried briefly under high vacuum
Sources & evidence
- ORD record
- ord-fd33494afdce4e27b48547056f70a984
- Source dataset
- uspto-grants-2003_09
- Patent number
- US06627648B1
Reaction notes
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