Reaktion #1467205
ord-210e1440237348e5a50da9dfab1c7eea
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Sonstigeozonised at -70° C.
- 2Temperaturthe latter is warmed to 0°-5° C
- 3Sonstigethe aqueous phase is separated off
- 4Waschenthe organic phase is washed with water
- 5Trocknendried over magnesium sulphate
- 6workup.DISSOLUTIONThe crude product is dissolved in 3 ml of methylene chloride
- 7workup.ADDITION15 ml of toluene are added
- 8FiltrationThe precipitate is filtered off
- 9Sonstigethe filtrate is evaporated in vacuo
- 10SonstigeThe residue is recrystallised from mthanol
Vorschrift
(di) The crude 2-[4-(p-toluenesulphonylthio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methylenebutyric acid p-nitrobenzyl ester, obtained according to Example 1cvii), is dissolved in 20 ml of methyl acetate and ozonised at -70° C. until no further starting material is present, according to a thin layer chromatogram. A stream of nitrogen is then passed through the solution and the latter is warmed to 0°-5° C. A solution of 300 mg of sodium bisulphite in 5 ml of water is added and the mixture is stirred for about 5 minutes until no further ozonide can be detected with potassium iodide/starch paper. The mixture is diluted with ethyl acetate, the aqueous phase is separated off, and the organic phase is washed with water, dried over magnesium sulphate and freed from solvent in vacuo. The crude product is dissolved in 3 ml of methylene chloride and 15 ml of toluene are added. The precipitate is filtered off and the filtrate is evaporated in vacuo. The residue is recrystallised from mthanol and gives 2 -[4-(p-toluenesulphonylthio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-hydroxycrotonic acid p-nitrobenzyl ester of melting point 159°-160° C.