Reaktion #54376

Reaktionsgleichung

toluene ethyl acetate

2-[4-(benzoxazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methylene-butyric acid diphenylmethyl ester

ozone

O2 O3

→

2-[4-(Benzoxazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-hydroxy-crotonic acid diphenylmethyl ester

Lösungsmittel

ethyl acetate

Reaktionsbedingungen

Aufarbeitung

1. 1
   EinengenThe solution is concentrated by evaporation to about 50 ml in vacuo
2. 2
   workup.ADDITIONmixed with 5 ml of dimethyl sulphide
3. 3
   Sonstigeno longer gives
4. 4
   Sonstigea reaction
5. 5
   EinengenThe mixture is concentrated by evaporation in vacuo
6. 6
   workup.DISSOLUTIONthe residue is dissolved in 150 ml of benzene
7. 7
   Waschenthe solution is washed with water
8. 8
   TrocknenThe organic phase is dried over sodium sulphate
9. 9
   Einengenconcentrated by evaporation
10. 10
    SonstigeThe residue is chromatographed on 150 g of acid-washed silica gel

Vorschrift

(aix) Approximately one equivalent of ozone (in the form of an O2 /O3 mixture) is passed into a solution, cooled to -70° C., of 3.35 g of 2-[4-(benzoxazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methylene-butyric acid diphenylmethyl ester in 125 ml of ethyl acetate, until starting material is no longer detectable by thin layer chromatography (silica gel; toluene/ethyl acetate, 3:1). The solution is concentrated by evaporation to about 50 ml in vacuo, mixed with 5 ml of dimethyl sulphide and stirred until the potassium iodide/starch test no longer gives a reaction. The mixture is concentrated by evaporation in vacuo, the residue is dissolved in 150 ml of benzene and the solution is washed with water. The organic phase is dried over sodium sulphate and concentrated by evaporation. The residue is chromatographed on 150 g of acid-washed silica gel, using toluene/ethyl acetate, 4:1. 2-[4-(Benzoxazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-hydroxy-crotonic acid diphenylmethyl ester is obtained in the form of a white foam; IR spectrum (methylene chloride): characteristic bands at 5.60, 5.90 and 6.0 μ.

Quelle