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3,5:4,6-受保护的L-或D-古龙酸的衍生物的方法,其在制备2-酮基-L-或D-古龙酸或其酯或L-或D-抗坏血酸中的用途,以及某些新型2-硝酸古洛糖酸酯中间体

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 contecting L- or D-gulono-1,4-lactone with an aldehyde 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L-或D-古洛糖醛酸的3,5:4,6-保护的衍生物是通过用醛二烷基缩醛对L-或D-古洛糖醇-1,4-内酯进行保护来制备的,或在存在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DE2860399D1

    专利类型

  • 公开/公告日1981-02-26

    原文格式PDF

  • 申请/专利权人 PFIZER INC.;

    申请/专利号DE19782860399T

  • 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 DE

  • 入库时间 2022-08-22 15:16:57

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