首页> 外国专利> Forming hydroxy-ester, useful to prepare hydroxy-acids that are useful in cosmetic field, comprises reacting phosphonate compound with lactol by Wittig-Horner reaction and subjecting ester under saponification reaction to give hydroxy-acid

Forming hydroxy-ester, useful to prepare hydroxy-acids that are useful in cosmetic field, comprises reacting phosphonate compound with lactol by Wittig-Horner reaction and subjecting ester under saponification reaction to give hydroxy-acid

机译:形成用于制备在化妆品领域中有用的羟基酸的羟基酯,包括使膦酸酯化合物与乳酸酯通过Wittig-Horner反应与酯反应,并使酯在皂化反应下产生羟基酸。

摘要

Preparation of hydroxy-ester compound (I) comprises reacting a phosphonate compound with a lactol compound by Wittig-Horner reaction to give (I) and subjecting (I) under saponification reaction to obtain a hydroxy-acid. Preparation of hydroxy-ester compound (I) of formula HO-CH 2-(CH 2) n-CH=C(R1)-C(=O)(OR3) comprises reacting a phosphonate compound of formula P(=O)((R2O) 2)-CH(R1)-C(=O)(OR4) with a lactol compound of formula (II) by Wittig-Horner reaction to give (I) and subjecting (I) under saponification reaction to obtain a hydroxy-acid of formula HO-CH 2-(CH 2) n-CH=C(R1)-C(=O)(OH). R3 : H or 1-6C alkyl, preferably ethyl; R1 : H, F, Cl, Br, CF 3 or 1-6C alkyl (optionally substituted by halo); n : greater than 4, preferably =6; either R2 : 1-6C alkyl, preferably ethyl or methyl; or R2OP : a cyclic ring; and R4 : 1-6C alkyl, preferably ethyl. Provided that when R1 is hydrogen, then the reaction is carried out by Doebner-knoevenagel reaction using a malonic acid derivative of formula R 3OOC-CH 2-COOR 3. An independent claim is included for (I) obtained by the process. [Image].
机译:羟基酯化合物(I)的制备包括通过Wittig-Horner反应使膦酸酯化合物与乳醇化合物反应,得到(I),然后在皂化反应下使(I)得到羟基酸。式HO-CH 2-(CH 2)的羟基酯化合物(I)的制备n-CH = C(R1)-C(= O)(OR3)包括使式P(= O)( (R2O)2)-CH(R1)-C(= O)(OR4)与式(II)的内酯化合物通过Wittig-Horner反应制得(I)并在皂化反应下进行(I)以获得羟基-式HO-CH 2-(CH 2)n -CH = C(R 1)-C(= O)(OH)的酸。 R3:H或1-6C烷基,优选乙基; R1:H,F,Cl,Br,CF 3或1-6C烷基(任选被卤素取代); n:大于4,优选≥6; R2:1-6C烷基,优选乙基或甲基;或R2OP:环; R 4:1-6C烷基,优选乙基。假设当R 1为氢时,则使用式R 3OOC-CH 2 -COOR 3的丙二酸衍生物通过Doebner-knoevenagel反应进行反应。(I)包括通过该方法获得的独立权利要求。 [图片]。

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