تفاعل #214640
ord-de20d7449bb049aa8a8941f1cae6cff4
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1تركيزThe solution is concentrated by evaporation to about 50 ml in vacuo
- 2workup.ADDITIONmixed with 5 ml of dimethyl sulphide
- 3أخرىno longer gives
- 4أخرىa reaction
- 5تركيزThe mixture is concentrated by evaporation in vacuo
- 6workup.DISSOLUTIONthe residue is dissolved in 150 ml of benzene
- 7غسيلthe solution is washed with water
- 8تجفيفThe organic phase is dried over sodium sulphate
- 9تركيزconcentrated by evaporation
- 10أخرىThe 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.