Reacción #1061905

ord-2ebe7baa94d343c48296cfef53694823

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe Fulcat 22B catalyst is then removed by filtration and excess p-xylene
  2. 2
    Otrois removed by distillation on a vacuum rotary evaporator
  3. 3
    OtroCrystallisation of the residue from 400 ml of methanol

Procedimiento

To a solution of 262.3 g (1.00 mol) of 5,7-di-tert-butyl-3-hydroxy-3H-benzofuran-2-one (compound (201), Table 2, Example 1a) in 500 ml (4.05 mol) of p-xylene are added 40 g of Fulcat 22B and the mixture is refluxed for 1.5 hours on a water separator. The Fulcat 22B catalyst is then removed by filtration and excess p-xylene is removed by distillation on a vacuum rotary evaporator. Crystallisation of the residue from 400 ml of methanol yields 280.6 g (80%) of 5,7-di-tert-butyl-3-(2,5-dimethylphenyl)-3H-benzofuran-2one, m.p. 93°-97° C. (compound (101), Table 1).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05607624uspto-grants-1997_03