Reacción #74753

ord-594ea544cd3e4ecf976a92c8aafa37d0

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe product separates during the course of the reaction (5 hours at 35°-38°)
  2. 2
    OtroCrystallization (of 9.7 g) from 70 ml of MeCN
  3. 3
    Otrogives 8.8 g (86%) of nearly colorless solid

Procedimiento

Ten grams (0.039 mole) of 2-(p-chlorobenzylidene)-1-indanone is converted to the epoxide in 1 liter of MeOH, using 9.6 g (0.085 mole) of 30% H2O2 and 9.6 ml (0.039 mole) of 16% NaOH, as described in Example 1. Since the starting material is poorly soluble in MeOH it is oxidized as a suspension and the product separates during the course of the reaction (5 hours at 35°-38°). The crude yield is 10 g (94%); m.p. 162°-164°. Crystallization (of 9.7 g) from 70 ml of MeCN gives 8.8 g (86%) of nearly colorless solid; m.p. 165°-167°.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04173634uspto-grants-1979_11