Reacción #463649

ord-2142058c6b9d4f65bbba617e9cf0cfd1

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaAfter cooling of the reaction mixture creamy crystals
  2. 2
    Otrowere separated by filtration
  3. 3
    Lavadowashed with ethyl ether
  4. 4
    Otrodried

Procedimiento

4-styrylpyridine (1.81 g) and 2-(2-bromoethyl) 1,3-dioxane (1.95 g) were stirred and refluxed in ethylacetate (15 ml) solution for 15 hours. After cooling of the reaction mixture creamy crystals were separated by filtration, washed with ethyl ether and dried to give 3.4 g of N-[2-(1,3-dioxane-2-yl)ethyl]-4-styrylpyridinium bromide.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06020436uspto-grants-2000_02