Reaktion #2224

ord-a3d67c3bad7c44c29b9bc8727026575d

Reaktionsgleichung

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
Ausbeute 48.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas refluxed overnight
  2. 2
    Temperaturcooled
  3. 3
    Filtrationfiltered
  4. 4
    WaschenThe light yellow solid was washed with hexane
  5. 5
    Sonstigedried

Vorschrift

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).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05728698uspto-grants-1998_03