拆分法制L-2-哌啶酸  

Enantiomeric Separation of DL-pipecolinic Acid

作　　者：李传润[1] 王丹[1] 胡海霞[1] 

机构地区：[1]安徽中医学院药学系,合肥230038

出　　处：《安徽化工》2002年第6期20-21,共2页Anhui Chemical Industry

摘　　要：以dl-2-哌啶酸为原料通过拆分制得L-2-哌啶酸。用D-(-)-酒石酸与dl-2-哌啶酸成盐的化学法,结合选择吸附法和晶种结晶法制得纯度较高的单一异构体。制得L-2-哌啶酸总收率为70.8%,纯度为99.4%,可作为合成纯左旋体罗哌卡因的起始原料。化学成盐拆分法结合选择吸附法和晶种结晶法能制得高纯单一异构体。L-pipecolinic acid was manufactured with dl-pipecolinic acid as primary materi al. The methods included chemical method of the incorporation of D---tartaric acsid and dl-pipecolinic acid selective adsorpt ion and seeded growth crystallization.The purity of the product was 99.4% and it was suitable for the synthesis of ropivacaine. The methods was practicable to gain single isomeride with a high purity.

关 键 词：拆分法 制备 L-2-哌啶酸 罗哌卡因 晶种结晶 药物 

分 类 号：TQ465.54[化学工程—制药化工]