Hexane → HCID 23078353, compound

HRID 228817

Reaction equation

HRID 228817 reaction equation
Br[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[N:3]=1.CCCCCC.C([Li])CCC.[CH3:20][C:21]1[CH:22]=[C:23]([O:26][C:27]=1[CH3:28])[CH:24]=[O:25]>O1CCCC1.O>[CH3:20][C:21]1[CH:22]=[C:23]([CH:24]([C:2]2[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[N:3]=2)[OH:25])[O:26][C:27]=1[CH3:28]

Participants

7

Conditions

Temperature
-78 °C

Procedure

2-Bromo-6-picoline (1.5 g) was dissolved in tetrahydrofuran (40 ml) under an argon atmosphere to prepare a solution. A 1.6 M hexane solution (5.6 ml) of n-butyllithium was added dropwise to the solution at −78° C., and the mixture was then stirred at −78° C. for 30 min. A solution of 4,5-dimethylfurfural (1 g) in tetrahydrofuran (20 ml) was added dropwise thereto, and the temperature of the mixture was raised to room temperature while stirring. Water was added to the reaction solution to stop the reaction, and the solvent was removed by distillation under the reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using hexane-acetone to give (4,5-dimethylfuran-2-yl)-(6-methyl-pyridin-2-yl)-methanol (1.4 g, yield 74%).

Workup

  1. customto prepare a solution
  2. temperaturethe temperature of the mixture was raised to room temperature
  3. stirringwhile stirring
  4. customthe reaction
  5. customthe solvent was removed by distillation under the reduced pressure
  6. additionWater was added to the residue
  7. extractionthe mixture was extracted with ethyl acetate
  8. washThe ethyl acetate layer was then washed with water
  9. dry with materialwas dried over anhydrous sodium sulfate
  10. customThe solvent was removed by distillation under the reduced pressure
  11. customthe residue was purified by column chromatography

Sources & evidence

ORD record
ord-184fa0e40e7b4fb6846e0d92c287f54f
Source dataset
uspto-grants-2009_07
Patent number
US07560558B2

Linked notes

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