首页> 外国专利> METHOD FOR PRODUCING SURFACE-ACTIVE SUBSTANCES BASED ON N-ACYLAMIN ACID WITH APPLICATION OF SURFACE-ACTIVE SUBSTANCES BASED ON N-ACYLAMIN ACID OR CORRESPONDING ANHYDRIDES IN ACCIDENTS

METHOD FOR PRODUCING SURFACE-ACTIVE SUBSTANCES BASED ON N-ACYLAMIN ACID WITH APPLICATION OF SURFACE-ACTIVE SUBSTANCES BASED ON N-ACYLAMIN ACID OR CORRESPONDING ANHYDRIDES IN ACCIDENTS

机译:一种基于N-乙酰氨基丙酸或相应的酸酐的表面活性物质的制备基于N-乙酰氨基磺酸的表面活性物质的方法

摘要

1. A method for producing N-acylamino acid-based surfactants of formula I, formula I, wherein R is selected from a C-C alkyl group, R is selected from H, C-C alkyl, R is selected from all groups at the α-carbon atom of natural amino acids, R is selected from COOX, CH-SOX, X is selected from Li, Na or K; the process comprises the steps of A) producing fatty acid chlorides by halogenating the fatty acids with thionyl chloride in the presence of a catalytic amount of the same or different N-acylamino acid-based surfactant of the formula I or anhydrides t the same surfactant of formula II, formula II, where R represents a C-C 1-6 alkyl group, R 1 represents H, C 1 -C 6 alkyl, R 1 represents all groups at the α-carbon atom of natural amino acids, n is from 0 to 4, X represents C, SO, and B) the reaction of the fatty acid chloride from step (A) with an amino acid in the presence of a base under the usual Schotten-Baumann aqueous conditions. 2. A method according to claim 1, wherein the catalytic amount of the compounds of formula I and formula II is from 0.05 to 0.5% by weight of a fatty acid. The method according to claim 1, wherein the amino acids used in the synthesis of compounds of formula I are selected from naturally occurring α-amino acids. The method of claim 3, wherein naturally occurring α-amino acids are selected from glycine, alanine, valine, leucine, isoleucine, methionine, proline, cysteine, phenylalanine, tyrosine, tryptophan, arginine, lysine, histidine, aspartic acid, glutamic acid, serine, threonine, aspergin and glutamine. 5. A method according to claim 1, wherein the amino acids used in the synthesis of compounds of formula I are selected from non-naturally occurring amino acids and mixtures of stereoisomers. The method of claim 5, wherein
机译:1.一种制备基于式I,式I的N-酰基氨基酸的表面活性剂的方法,其中R选自CC烷基,R选自H,CC烷基,R选自α-碳上的所有基团。天然氨基酸的原子,R选自COOX,CH-SOX,X选自Li,Na或K;该方法包括以下步骤:A)在催化量的相同或不同的式I的基于N-酰基氨基酸的表面活性剂或与该相同的表面活性剂的酸酐存在下,通过用亚硫酰氯卤化脂肪酸来生产脂肪酸氯化物。式II,式II,其中R代表C 1-6烷基,R 1代表H,C 1 -C 6烷基,R 1代表天然氨基酸的α-碳原子上的所有基团,n为0至1。在图4中,X代表C,SO和B)在碱的存在下,在通常的Schotten-Baumann水性条件下,步骤(A)的脂肪酸氯化物与氨基酸的反应。 2.根据权利要求1的方法,其中式I和式II化合物的催化量为0.05-0.5重量%的脂肪酸​​。 2.根据权利要求1的方法,其中用于合成式I化合物的氨基酸选自天然存在的α-氨基酸。 4.权利要求3的方法,其中天然存在的α-氨基酸选自甘氨酸,丙氨酸,缬氨酸,亮氨酸,异亮氨酸,蛋氨酸,脯氨酸,半胱氨酸,苯丙氨酸,酪氨酸,色氨酸,精氨酸,赖氨酸,组氨酸,天冬氨酸,谷氨酸,丝氨酸,苏氨酸,曲霉毒素和谷氨酰胺。 5.根据权利要求1的方法,其中用于合成式I化合物的氨基酸选自非天然存在的氨基酸和立体异构体的混合物。 6.根据权利要求5所述的方法,其中,

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