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40 results about "Succinimide derivatives" patented technology

Polyaspartic acid derivative and synthetic method thereof

InactiveCN107602858APrevent the growth of the main chainIncreased side chain branching rateSide chainPhosphoric acid
The invention provides a polyaspartic acid derivative synthetic method. The method comprises the following steps: monosaccharide or disaccharide and monochloro acetic acid are reacted under catalysisof NaOH, and a reactant is subjected to further acidifying and purification to obtain carboxymethyl saccharide; carboxymethyl saccharide and diamine are subjected to dehydration condensation under catalysis of phosphoric acid to obtain glycosyl acetyl diamine; L-aspartic acid and phosphoric acid are respectively added in a kneading reactor for mixing, a mixture is stirred and heated, polymerization is carried out for preset time to obtain polysuccinimide; glycosyl acetyl diamine is added in a reaction vessel of polysuccinimide for a reaction, polysuccinimide is subjected to ring-opening and grafting reaction to obtain a polysuccinimide derivative; the polysuccinimide derivative is added in a hydrolysis kettle, an aqueous solution of alkali is add drop by drop, a hydrolysis reaction is carried out, and a liquid-phase product after hydrolysis is a glycosyl acetyl diamine-grafted modified polyaspartate aqueous solution. The synthetic method is simple and easy to operate, a grafting modification step and a polymerization step are coupled, so that the side-chain grafting rate is increased and the polymericular weight can be regulated and controlled.
Owner:苏州美瑞姿生物科技有限公司

Method for synthesizing polyaspartic acid derivative through multi-component evaporative crystallization copolymerization modification

The invention discloses a method for synthesizing polyaspartic acid derivative through multi-component evaporative crystallization copolymerization modification, relates to a method for synthesizing the polyaspartic acid, and solves the technical problems of large particle diameter of polyaspartic acid particles, high crystallinity and low scale inhibition rate of the polyaspartic acid prepared with the conventional solid-phase pyrocondensation polymerization method. The method comprises the following steps of: pretreating: dissolving L-aspartic acid and L-serine in distilled water, heating to separate solid out and drying to obtain a sample; heating the sample and reacting under stirring to obtain a polysuccinimide derivative; cooling to room temperature and dropwise adding a sodium hydroxide aqueous solution to obtain a polyaspartic acid sodium salt solution; dropwise adding a hydrochloric acid solution and absolute ethanol until precipitate is obtained; standing to remove supernatant; and drying precipitate in a drying box to constant weight so as to obtain the polyaspartic acid derivative, wherein the yield of the sample obtained by pretreatment reaches 95-100 percent, the particle diameter of the particles is small, and the crystallinity is high. The polyaspartic acid derivative has the scale inhibition rate of 92-93 percent and is applied to the field of scale inhibitors.
Owner:HEILONGJIANG UNIV

Synthesis method and application of PASP derivative with surface activity

The invention discloses a synthesis method of a PASP derivative with surface activity. The synthesis method comprises the following steps: s1, synthesizing polysuccinimide; s2, synthesizing a polysuccinimide derivative grafted and modified by alkyl primary amine; s3, adding the alkyl primary amine modified polysuccinimide derivative into a hydrolysis kettle, adding water of which the mass is 3-6 times that of the polysuccinimide derivative, stirring and dispersing, slowly dropwise adding 2-5mol/L NaOH solution for hydrolysis under the heating and stirring maintaining conditions, and hydrolyzing at 35-65 DEG C for 2-6h to obtain a hydrolysate, namely an alkyl primary amine graft modified polyaspartate aqueous solution; and carrying out pH adjustment, filtration, ultrafiltration, concentration and purification for further refining. The method is simple and easy to operate, and the polymerization degree and the grafting rate are regulated and controlled by regulating and controlling the proportion and the chain length of the added alkyl primary amine compound. The synthesized alkyl primary amine modified polyaspartic acid derivative has excellent surface activity and chelating property, and has the effects of moisturizing, removing freckles, whitening, improving skin, removing heavy metals and the like.
Owner:苏州美瑞姿生物科技有限公司

Electrochemical synthesis method of 2, 2-bissuccinimide derivative

The invention provides an electrochemical synthesis method of a 2, 2 '-bis-succinimide derivative, which is characterized in that an organic solvent in which a maleimide derivative is dissolved is used as an electrolytic reaction raw material, and the 2, 2'-bis-succinimide derivative is synthesized under an electrolytic condition. Compared with traditional organic synthesis, the electrochemical method for synthesizing the 2, 2 '-bissuccinimide derivative has remarkable advantages, the electrochemical reaction is realized by obtaining and losing electrons from reactants on an electrode, additional reducing agents or metal catalysts are not needed, material consumption is reduced, and therefore environmental pollution is reduced; the reaction can be carried out at room temperature and normal pressure, the reaction condition is mild, and the post-treatment is simple, which is very beneficial to energy conservation and equipment investment reduction; the process flow is simple, the operation is simple and convenient, the reaction is easy to control, and the 2, 2 '-bissuccinimide derivative can be obtained through one-pot reaction; the reaction raw materials are cheap and easily available, and are very safe to use; the reaction process is environment-friendly and meets the requirements of an environment-friendly chemical process.
Owner:ZHEJIANG UNIV OF TECH

Process for producing optically active succinimide derivatives and intermediates thereof

A process for producing optically active succinimide derivatives as key intermediates of (3R)-2′-(4-bromo-2-fluorobenzyl)spiro{pyrrolidine-3,4′(1H)-pyrrolo[1,2-a]pyrazine}-1′,2,3′,5(2′H)-tetraone, which comprises the following reaction steps.
Owner:KYOWA HAKKO BIO CO LTD +1
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