Reacción #1198

Ecuación de reacción

tetradecanol

NaH

methallyl chloride

m-chloroperbenzoic acid

→

1,2-epoxy-2-methyl-3-tetradecyloxypropane

Rendimiento 79.5%

Disolventes

water

dimethylformamide

dichloromethane

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroA 200-ml flask equipped with a stirrer
2. 2
   OtroAfter completion of the reaction
3. 3
   Extracciónsubjected to extraction with hexane
4. 4
   workup.DISTILLATIONthe solvent was distilled off under reduced pressure
5. 5
   workup.ADDITIONThe resultant residue was charged into a 300-ml flask
6. 6
   Otroequipped with a stirrer
7. 7
   OtroSolids formed
8. 8
   Otrowere separated by filtration
9. 9
   Concentraciónthe resultant solution was concentrated under reduced pressure
10. 10
    Otropurified by column chromatography on silica gel

Procedimiento

A 200-ml flask equipped with a stirrer was charged with 10 g (46.6 mmol) of tetradecanol, 50 ml of dimethylformamide, 2.86 g (71.5 mmol) of 60% NaH and 5.96 g (65.8 mmol) of methallyl chloride. The contents were stirred at 60° C. for 15 hours. After completion of the reaction, the reaction mixture was added with water and subjected to extraction with hexane, and the solvent was distilled off under reduced pressure. The resultant residue was charged into a 300-ml flask equipped with a stirrer, and 12.24 g (70.9 mmol) of m-chloroperbenzoic acid and 200 ml of dichloromethane were added thereto. The resultant mixture was stirred at room temperature for 19 hours. Solids formed were separated by filtration, and the resultant solution was concentrated under reduced pressure and then purified by column chromatography on silica gel, thereby obtaining 10.54 g (yield: 79.4%) of 1,2-epoxy-2-methyl-3-tetradecyloxypropane as an intermediate.

Fuente