发明名称 UN PROCEDIMIENTO PARA LA RECUPERACIËN DE CEFALOSPORINA C
摘要 Cephalosporin C is recovered from a clarified beer containing it and co-present Cephalosporin N by lowering the pH of the clarified beer preferably adjusted to pH5-6 with acetic acid or sodium hydroxide by treatment with a cation exchange material containing strong acidic groups in hydrogen form to a value of from 2.8 to 4.0, separating the cation exchange material from the acidified medium, then passing the acidified medium through a strong anion exchange material in the form of a salt of a weak monobasic organic acid e.g. acetic acid to remove substantially all chloride and other inorganic anions therefrom and thereafter separating the Cephalosporin C from the percolate. The Cephalosporin C may be separated from the percolate by contacting it with an anion exchange material in the form of a salt of a weak monobasic organic acid e.g. acetic acid to adsorb the Cephalosporin C thereon and eluting the adsorbed Cephalosporin C therefrom with acetic or formic acid which, in the case where the anion exchange material is a weak anion exchange material is buffered by the addition of a weak base which is volatile enough to be removed by distillation in vacuo from aqueous solution at a temperature below the decomposition temperature of Cephalosporin C e.g. pyridine or ammonia. The Cephalosporin C may be precipitated from the eluate by acetone, dissolved in water and converted to its sodium salt by treatment with sodium hydroxide or a strong cation exchange resin in sodium form. The removal of chloride and other anions may be effected by a plurality of sections of strong anion exchange material. The Cephalosporin C may be separated from the percolate by adsorption on alumina or charcoal and elution therefrom. Specification 810,196 is referred to.
申请公布号 ES264299(A1) 申请公布日期 1961.06.01
申请号 ES19610264299 申请日期 1961.01.24
申请人 NATIONAL RESEARCH DEVELOPMENT CORPORATION 发明人
分类号 B01J47/00;C07D501/12;C12P35/06 主分类号 B01J47/00
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