Reacción #54376

ord-3fab32337586442b92eb3c0de3aab9c8

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe solution is concentrated by evaporation to about 50 ml in vacuo
  2. 2
    workup.ADDITIONmixed with 5 ml of dimethyl sulphide
  3. 3
    Otrono longer gives
  4. 4
    Otroa reaction
  5. 5
    ConcentraciónThe mixture is concentrated by evaporation in vacuo
  6. 6
    workup.DISSOLUTIONthe residue is dissolved in 150 ml of benzene
  7. 7
    Lavadothe solution is washed with water
  8. 8
    SecadoThe organic phase is dried over sodium sulphate
  9. 9
    Concentraciónconcentrated by evaporation
  10. 10
    OtroThe residue is chromatographed on 150 g of acid-washed silica gel

Procedimiento

(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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04147864uspto-grants-1979_04