首页> 外国专利> Process for preparing 3,5:4,6- protected derivatives of L- or D- gulonic acid, their use in preparing 2- keto-L- or D- gulonic acid or their esters or L- or D- ascorbic acid, and certain novel 2-nitrato-gulonate intermediates

Process for preparing 3,5:4,6- protected derivatives of L- or D- gulonic acid, their use in preparing 2- keto-L- or D- gulonic acid or their esters or L- or D- ascorbic acid, and certain novel 2-nitrato-gulonate intermediates

机译:制备L-或D-古洛糖酸的3,5:4,6-保护的衍生物的方法,其在制备2-酮基-L-或D-古洛糖酸或其酯或L-或D-抗坏血酸中的用途,以及某些新颖的2-硝基古洛糖酸盐中间体

摘要

The invention relates to a process in which a 3,5:4,6-protected derivative of L- or D-glulonic acid is prepared by contacting L- or D-gulono-1,4-lactone with an aldehvde dialkyl acetal, or with an aldehyde and an alcohol, in the presence of an acid having a pKa of less than 3. This protected derivative may be oxidised and hydrolysed to 2-keto-L- or D-gulonic acid or ester thereof, which in turn may be hydrolysed to L- or D-ascorbic acid. L-ascorbic acid is of course Vitamin C. The invention also relates to the novel intermediates produced by the above processes.
机译:本发明涉及一种方法,其中通过使L-或D-古洛诺-1,4-内酯与醛缩二烷基乙缩醛接触来制备L-或D-古洛糖醛酸的3,5:4,6-保护的衍生物。在存在pKa小于3的酸的情况下,用醛和醇将其氧化,然后将其水解为2-酮基-L-或D-古洛糖酸或其酯,然后依次为水解为L-或D-抗坏血酸。 L-抗坏血酸当然是维生素C。本发明还涉及通过上述方法生产的新型中间体。

著录项

  • 公开/公告号EP0000243A1

    专利类型

  • 公开/公告日1979-01-10

    原文格式PDF

  • 申请/专利权人 PFIZER INC.;

    申请/专利号EP19780300017

  • 发明设计人 CRAWFORD THOMAS CHARLES;

    申请日1978-06-05

  • 分类号C07D307/62;C07H7/02;C07H9/04;C07D493/04;

  • 国家 EP

  • 入库时间 2022-08-22 20:07:57

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号