تفاعل #214640

ord-de20d7449bb049aa8a8941f1cae6cff4

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe solution is concentrated by evaporation to about 50 ml in vacuo
  2. 2
    workup.ADDITIONmixed with 5 ml of dimethyl sulphide
  3. 3
    أخرىno longer gives
  4. 4
    أخرىa reaction
  5. 5
    تركيزThe mixture is concentrated by evaporation in vacuo
  6. 6
    workup.DISSOLUTIONthe residue is dissolved in 150 ml of benzene
  7. 7
    غسيلthe solution is washed with water
  8. 8
    تجفيفThe organic phase is dried over sodium sulphate
  9. 9
    تركيزconcentrated by evaporation
  10. 10
    أخرىThe residue is chromatographed on 150 g of acid-washed silica gel

الإجراء التجريبي

(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 6.0μ.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04255328uspto-grants-1981_03