Methyl iodide → 2-Ethyl-6-methylpyridine

HRID 1499334Notes

Reaction equation

HRID 1499334 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[N:3]=1.[CH2:9](N(CC)CC)C.C([Li])CCC.CI>CCCCCC.O1CCCC1>[CH2:1]([C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[N:3]=1)[CH3:9]

Participants

7

Conditions

Temperature
-40 °C

Procedure

In a 250-ml 3-neck jacketed reactor flask, 4.3 g (40.2 mmol) of 2,6-dimethylpyridine and 4.06 g (40.2 mmol) of triethylamine were dissolved by addition of 50 ml of anhydrous tetrahydrofuran, and the solution was cooled to −40° C., after which 28.7 ml (46 mmol) of 1.6 M n-butyllithium in hexane was added dropwise thereto. At the same time, the solution changed to deep red. Next, the solution was stirred for 1 hour, and then warmed to 0° C., after which 5.7 g (40.2 mmol) of methyl iodide was added dropwise thereto, followed by stirring for 1 hour. Then, the reaction product was concentrated, and the concentrate was dissolved in ethyl acetate, washed with water and saline, dried with anhydrous magnesium sulfate, and then concentrated again, thereby obtaining crude 2-ethyl-6-methylpyridine.

Workup

  1. temperaturewarmed to 0° C.
  2. stirringby stirring for 1 hour
  3. concentrationThen, the reaction product was concentrated
  4. dissolutionthe concentrate was dissolved in ethyl acetate
  5. washwashed with water and saline
  6. dry with materialdried with anhydrous magnesium sulfate
  7. concentrationconcentrated again

Sources & evidence

ORD record
ord-ebc788da9c0e431f9072b4ec70332cab
Source dataset
uspto-grants-2015_12
Patent number
US09200135B2

Reaction notes

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