Pyridine → Pyridinium, 1-dodecyl-, bromide (1:1)

HRID 980423Notes

Reaction equation

HRID 980423 reaction equation
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13].[N:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>C(O)(C)C>[Br-:1].[CH2:2]([N+:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13]

Participants

4

Procedure

Equimolar amounts of 1-bromo-dodecane (249.2 g) and pyridine (79.1 g) are placed in a glass, three-necked, round bottom flask equipped with a heating means, a stirring means, and a condensing means. Then 82.1 g of isopropanol are added to the flask as a solvent. The contents of the vessel are heated to reflux with constant stirring. Reflux is maintained for six hours. Analysis of the reaction mixture indicates that the reaction is approximately 100 percent complete.

Workup

  1. customthree-necked, round bottom flask equipped with a heating
  2. temperatureThe contents of the vessel are heated
  3. temperatureto reflux with constant stirring
  4. temperatureReflux
  5. temperatureis maintained for six hours

Sources & evidence

ORD record
ord-2faed7215f844b52838800e11d85d1f9
Source dataset
uspto-grants-1987_01
Patent number
US04637899

Reaction notes

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