Reacción #214315

ord-1ad4f162cba04b13afc719abe876680b

Ecuación de reacción

COC(CBr)OC
2-Bromo-1,1-dimethoxyethane
CC(O)CCO
1,3-butanediol
Cc1ccccc1S(=O)(=O)O
Toluene sulfonic acid
CC1CCOC(CBr)O1
2-bromomethyl-4-methyl-1,3-dioxane

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrofitted with a mechanical stirrer
  2. 2
    Temperaturathermometer, Dean Stark trap and reflux condenser
  3. 3
    Temperaturathe reaction mixture is heated
  4. 4
    Otroalcohol removed
  5. 5
    workup.ADDITIONtreated with sodium carbonate (5 grams)
  6. 6
    Filtraciónfiltered
  7. 7
    Otroa rotary evaporator

Procedimiento

2-Bromo-1,1-dimethoxyethane (0.1 mole) and 1,3-butanediol (0.1 mole) are charged into a glass reaction vessel fitted with a mechanical stirrer, thermometer, Dean Stark trap and reflux condenser. Toluene sulfonic acid (0.1 grams) is added and the reaction mixture is heated and alcohol removed. When alcohol evolution ceases, the reaction mixture is then cooled to room temperature, treated with sodium carbonate (5 grams) and filtered. Volatiles are stripped from the filtrate using a rotary evaporator to yield the desired product 2-bromomethyl-4-methyl-1,3-dioxane as the residue.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04255182uspto-grants-1981_03