Reacción #55465

ord-911ca978e7994602922686e1b9d8dd0d

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónthe mixture is concentrated by evaporation in vacuo
  2. 2
    OtroThe solid residue is triturated with petroleum ether
  3. 3
    Otroto obtain 27.4 g (95% of theory) of the above compound in the form of light-yellow crystals, m.p. 95°-96°

Procedimiento

27.2 g of N-(3',4'-dichlorophenyl)-3,4-dimethyl-2-hydroxy-5-oxo-2,5-dihydropyrrole (see Example 3) is added to 25 ml of thionyl chloride, with an intense evolution of gas occurring. After being stirred for one hour at 50°, the mixture is concentrated by evaporation in vacuo. The solid residue is triturated with petroleum ether to obtain 27.4 g (95% of theory) of the above compound in the form of light-yellow crystals, m.p. 95°-96°.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04220655uspto-grants-1980_09