Reacción #1610

ord-3b6843caea374b8d88ee79ad8d8db495

Ecuación de reacción

O=C(CBr)c1ccc(Cl)cc1
2-bromo-p-chloroacetophenone
COC(=S)NN
methoxythiocarbonylhydrazine
O=C1NN=C(c2ccc(Cl)cc2)CS1
5-(4-chlorophenyl)-3H,6H-1,3,4-thiadiazin-2-one
Rendimiento 48.4%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas refluxed overnight
  2. 2
    Temperaturacooled
  3. 3
    Filtraciónfiltered
  4. 4
    LavadoThe light yellow solid was washed with hexane
  5. 5
    Otrodried

Procedimiento

A mixture of 2-bromo-p-chloroacetophenone (9.16 g), methoxythiocarbonylhydrazine (13.0 g) and acetonitrile (75 ml) was refluxed overnight and then cooled and filtered. The light yellow solid was washed with hexane and dried yielding 5-(4-chlorophenyl)-3H,6H-1,3,4-thiadiazin-2-one (4.3 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726162uspto-grants-1998_03