2-Chloropyridine → Butyl 2-pyridyl ether

HRID 1769270Notes

Reaction equation

HRID 1769270 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

4

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

  1. temperatureheated for 2 hours
  2. temperatureAfter cooling
  3. customprecipitated sodium chloride
  4. customwas removed
  5. filtrationby filtering
  6. washthe residue was washed with about 500 ml of n-butanol
  7. distillationThe combined filtrates were distilled in vacuum
  8. 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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