Réaction #49994
ord-4eddb2e4e3b64314ab38ee9674cdc374
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Traitement
- 1workup.STIRRINGby stirring for 0.5 hour
- 2AutreAn insoluble material was removed by filtration over celite
- 3Lavagewashed 3 times with ethyl acetate (20 ml)
- 4Autrethe aqueous layer was separated from the organic layer
- 5Extractionextracted with ethyl acetate (200 ml)
- 6Lavagewashed with brine
- 7Séchagedried over anhydrous sodium sulfate
- 8FiltrationAfter filtration
- 9Concentrationthe filtrate was concentrated in vacuo
- 10Autrethe concentrate was crystallized from a mixture of toluene and n-hexane (1:1)
Mode opératoire
To a solution of (3S,4S)-4-(1-chloromethyl-ethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone (20 g) in dimethylsulfoxide (160 ml), there were successively added water (40 ml), cuprous oxide (6.76 g) and p-toluenesulfonic acid (7.6 g), and the resultant mixture was warmed to 50° to 55° C. and stirred for 2 hours at the same temperature. After cooling down to room temperature, 1% aqueous phosphoric acid (90 ml) and ethyl acetate (200 ml) were poured into the reaction mixture, followed by stirring for 0.5 hour. An insoluble material was removed by filtration over celite and washed 3 times with ethyl acetate (20 ml). The filtrate and the washings were combined together, and the aqueous layer was separated from the organic layer and extracted with ethyl acetate (200 ml). The organic layer and the extract were combined together, washed with brine and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated in vacuo, and the concentrate was crystallized from a mixture of toluene and n-hexane (1:1) to give crystals of (3S,4S)-4-(1-hydroxymethylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone. m.p., 118°-120° C.