Reacción #350141

ord-ef6bdfb48bb0487f9235881473eab142

Ecuación de reacción

c1ccc2c(c1)OCO2
benzodioxolan
O=[N+]([O-])O
nitric acid
O=[N+]([O-])c1ccc2c(c1)OC(c1ccccc1)O2
product
O=[N+]([O-])c1ccc2c(c1)OC(c1ccccc1)O2
5-nitro-2-phenyl-1,3-benzodioxolan

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted several times with acetic ester
  2. 2
    LavadoThe combined acetic ester phases were then washed several times with a solution of potassium bicarbonate
  3. 3
    Otroby drying
  4. 4
    Otroevaporation
  5. 5
    Concentraciónby concentration
  6. 6
    OtroCrystallization from ethanol

Procedimiento

A solution of 39.6 g (0.2 mol) of the benzodioxolan obtained as just described in 150 ml of acetic acid ester was added dropwise at 25° to 35° C. to 150 ml of a 33% nitric acid. The solution was poured into ice water after 2 hours and then extracted several times with acetic ester. The combined acetic ester phases were then washed several times with a solution of potassium bicarbonate and then with water, followed by drying and evaporation by concentration. Crystallization from ethanol furnished 37 g of a product of the melting point between 84° and 85° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04155915uspto-grants-1979_05