2-Chloropyridine → Butyl 2-pyridyl ether
Reaction equation
[OH-:1].[Na+].Cl[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][N:5]=1>C(O)CCC>[CH2:6]([O:1][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][N:5]=1)[CH2:7][CH2:8][CH3:9]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 112 °C
Procedure
Into a solution of 55 g (1,38 mole) of sodium hydroxide in 245 g of n-butanol heated to 100° C., were added dropwise over four hours 113.5 g (1 mole) of 2-chloropyridine and the mixture was stirred for about 15 hours at this temperature, then heated for 2 hours at reflux (ca. 112° C.). After cooling, precipitated sodium chloride was removed by filtering and the residue was washed with about 500 ml of n-butanol. The combined filtrates were distilled in vacuum and the first fraction to distill was a butanol-water azeotrope, then followed n-butanol and a 2-chloropyridine/n-butanol intermediate run. 2-butoxypyridine distilled last at 75° C. at 10 Torr as a colorless liquid to obtain 108 g (72%) of 2-butoxypyridine with a purity of >98%.
Workup
- temperatureheated for 2 hours
- temperatureAfter cooling
- customprecipitated sodium chloride
- customwas removed
- filtrationby filtering
- washthe residue was washed with about 500 ml of n-butanol
- distillationThe combined filtrates were distilled in vacuum
- distillationthe first fraction to distill
Sources & evidence
- ORD record
- ord-b7cf6ba17deb4eb0a990880af1a5d2a5
- Source dataset
- uspto-grants-1995_01
- Patent number
- US05380862
Reaction notes
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