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    • 3. 发明授权
    • Process for the preparation of (S)-glyceraldehyde acetonide
    • 制备(S) - 甘油醛缩酮的方法
    • US07361775B2
    • 2008-04-22
    • US10574693
    • 2004-10-07
    • Peter Jan Leonard Mario QuaedfliegFranciscus Alphons Marie LommenRobert Jan VijnDanniël Adrianus Franciscus Jacobus Boxtel Van
    • Peter Jan Leonard Mario QuaedfliegFranciscus Alphons Marie LommenRobert Jan VijnDanniël Adrianus Franciscus Jacobus Boxtel Van
    • C07D317/26
    • C07D317/26
    • The invention relates to a process for the preparation of (S)-glyceraldehyde acetonide in aqueous solution from 3,4-O-isopropylidene-L-threonic acid or a salt thereof in aqueous solution, and hypochlorite in aqueous solution wherein the aqueous hypochlorite solution has a pH>7.5 and wherein during addition of at least 0.1 molar equivalents of hypochlorite based on the amount of 3,4-O-isopropylidene-L-threonic acid, an acid solution is not simultaneously added. The invention also relates to a process according to the invention, wherein 3,4-O-isopropylidene-L-threonic acid or a salt thereof is prepared from 5,6-O-isopropylidene-L-ascorbic acid or a salt thereof in the presence of H2O2 and a base in a manner known per se, wherein excess H2O2 is optionally removed by catalase. The invention also relates to a process according to the invention, wherein 5,6-O-isopropylidene-L-ascorbic acid or a salt thereof is prepared by reacting L-ascorbic acid or a salt thereof with an acetonide forming agent, preferably in the presence of an acid catalyst.
    • 本发明涉及一种在水溶液中由3,4-O-异亚丙基-L-苏糖酸或其盐在水溶液中制备(S) - 甘油醛缩酮的方法,以及次氯酸盐水溶液中的次氯酸盐水溶液 pH> 7.5,其中基于3,4-O-异亚丙基-L-苏糖酸的量添加至少0.1摩尔当量的次氯酸盐,不能同时加入酸溶液。 本发明还涉及根据本发明的方法,其中3,4-O-异亚丙基-L-苏糖或其盐由5,6-O-异亚丙基-L-抗坏血酸或其盐在 以本身已知的方式存在H 2 O 2 O 2和碱,其中过量的H 2 O 2 O 2和/ 任选地被过氧化氢酶除去。 本发明还涉及根据本发明的方法,其中5,6-O-异亚丙基-L-抗坏血酸或其盐通过L-抗坏血酸或其盐与丙酮化物形成剂反应制备,优选在 存在酸催化剂。