Reacción #360843

ord-46302bb0417e4d80803efc7bded4318f

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas pumped through the CMR (18 ml/min; 160°-70° C.; 500 kPa;)
  2. 2
    Otrothe hot product collected in an ice-water cooled flask

Procedimiento

2-Acetylfuran (13.8 g), dimethylamine hydrochloride (13.3 g), paraformaldehyde (5.0 g) and ethanol (80 ml) acidified with concentrated HCl (1.0 ml) were stirred. Part of this mixture (27 ml) was pumped through the CMR (18 ml/min; 160°-70° C.; 500 kPa;) and the hot product collected in an ice-water cooled flask, to afford pale yellow crystals m.p. 172.5°-173° C. (cf lit.10 m.p. 173°-4° C.) in 13% yield.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05387397uspto-grants-1995_02