Reaktion #95841
ord-aad06569e85a4002a407f8718161f66a
Reaktionsgleichung
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Temperaturis heated
- 2Temperaturto reflux for 3 hours
- 3workup.WAITThe mixture is subsequently left
- 4Sonstigeto crystallise at 0° C.
- 5Filtrationthe separated solid material is filtered off under suction
- 6Sonstigetransferred to a separating funnel
- 7workup.ADDITION100 ml of chloroform and 25 ml of water are added
- 8SonstigeThen, the aqueous phase is separated
- 9WaschenThe organic phase is washed with 25 ml of water
- 10Trocknendried over sodium sulphate
- 11Sonstigeevaporated
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.