Reaktion #95841

ord-aad06569e85a4002a407f8718161f66a

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturis heated
  2. 2
    Temperaturto reflux for 3 hours
  3. 3
    workup.WAITThe mixture is subsequently left
  4. 4
    Sonstigeto crystallise at 0° C.
  5. 5
    Filtrationthe separated solid material is filtered off under suction
  6. 6
    Sonstigetransferred to a separating funnel
  7. 7
    workup.ADDITION100 ml of chloroform and 25 ml of water are added
  8. 8
    SonstigeThen, the aqueous phase is separated
  9. 9
    WaschenThe organic phase is washed with 25 ml of water
  10. 10
    Trocknendried over sodium sulphate
  11. 11
    Sonstigeevaporated

Vorschrift

A mixture of 33.2 g (0.1 mol) of diethyl (1,3,4,5-tetrahydro-4-methyl-5-oxo-2H-1,4-benzodiazepin-2-ylidene)malonate, 8.0 g (0.2 mol) of sodium hydroxide and 400 ml of absolute ethanol is heated to reflux for 3 hours. The mixture is subsequently left to crystallise at 0° C. and the separated solid material is filtered off under suction and transferred to a separating funnel. 100 ml of chloroform and 25 ml of water are added thereto. Then, the aqueous phase is separated. The organic phase is washed with 25 ml of water, dried over sodium sulphate and evaporated. There is obtained crystalline ethyl (1,3,4,5-tetrahydro-4-methyl-5-oxo-2H-1,4-benzodiazepin-2-ylidene)acetate of melting point 154°-155° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04346035uspto-grants-1982_08