Reacción #336387

ord-98389420ba7b4482934597b289074689

Disolventes

Condiciones de reacción

Temperatura
25°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction pressure
  2. 2
    FiltraciónThe precipitated crystals were filtered
  3. 3
    Lavadowashed with 30 ml of methyl alcohol
  4. 4
    Otrodried under reduced pressure

Procedimiento

A mixture comprising 10 g of the obtained 5-nitro-1,4-naphthoquinone, 3.3 g of 1,3-butadiene and 40 ml of ethylene glycol monomethyl ether was retained in a 100-milliliter autoclave at 50° C. for 6 hours with stirring. The reaction pressure was initially 1.2 atmospheres and 1.0 atmosphere when the reaction was over. Thereafter, 60 ml of water was added to the reaction mixture and cooled to 25° C. The precipitated crystals were filtered, washed with 30 ml of methyl alcohol and dried under reduced pressure to obtain 11.9 g of white 5-nitro-1,4,4a,9a-tetrahydroanthraquinone having a purity of 98%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05213665uspto-grants-1993_05