The amidation reaction between rapeseed oil and monoethanolamine was studied via orthogonal experiment.
通过正交实验对菜籽油与单乙醇胺的酰胺化反应进行了研究。
Oxidized wax is modified by amidation reaction to produce acylamide with better physical and chemical properties.
氧化蜡经过胺改性可以得到具有更佳物化性能的脂肪酸酰胺。
METHODS The title compound was synthesized from 5-amino-2,4, -6-triiodoisophthalic acid by acyl chlorination and amidation.
方法以5-氨基-2，4，6-三碘异酞酸为原料经酰氯化、酰胺化反应制得目标化合物。
By use of silane coupling agent KH550 the modified HBPE (MHBPE) was grafted onto the surface of ultrafine titanium dioxide by amidation reaction.
以硅烷偶联剂KH550为桥梁，利用酰胺化反应将改性的HBPE(记做MHBPE)接枝到超细二氧化钛表面。
The amidation and esterification of different cyclic anhydrides with aniline and phenol gave different major products, and the routes were optimized.
研究了环酐与苯胺和苯酚的酰胺化及酯化反应，优化了酰胺化及酯化反应条件。
METHODS The title compound was synthesized from 2-butene-1,4-diol, via esterification, epoxidation, amination, then amidation with tetraiodoterebenzoyl chloride.
方法以1，4-丁烯二醇为原料，经过酯化、环氧化、氨解开环，再与四碘对苯二甲酰氯反应合成目标产物。
A cationic protein filling agent has been prepared from collagen hydrolysate by amidation with ethanolamine and amination with diethanolamine-formaldehyde condensate.
采用乙醇胺对胶原水解物酰胺化，采用二乙醇胺与甲醛的缩合物胺化，制得了阳离子蛋白填充剂。
Introduces the research of synthesis alkanolamide sulfosuccinic acid monoester from refined corn oil by methyl-esterification, amidation, esterification and sulfonation.
介绍了以精制玉米油经甲酯化、酰胶化、酯化和磺化四步合成脂肪酸胺磷基琥珀酸单酯盐的研究。
Methods The substance was synthesized from P-hydroxybenzoic acid through three steps, those are etherification, preparation of acyl halide and amidation of the raw material.
方法以对羟基苯甲酸为原料，经三步合成，即原料的醚化、酰氯制备和酰胺化。
METHODS Cefsulodin was prepared, taking phenylacetic acid as the starting material, followed by sulfonation, resolution, acylation, amidation and substitution, in 5 steps totally.
方法以苯乙酸为原料，经磺化、拆分、酰化、酰胺化和取代五步反应合成头孢磺啶。
Levetiracetam was prepared from L-methionine via reduction-dethiomethylation, esterification, ammonolysis, amidation and intramolecular cyclocondensation reaction with 44.6% overall yield.
以蛋氨酸为原料经还原脱硫甲基化、酯化、氨解、酰胺化及分子内缩和成环4步反应合成得到了左乙拉西坦，总收率44.6%。
Levetiracetam was prepared from L-methionine via reduction-dethiomethylation, esterification, ammonolysis, amidation and intramolecular cyclocondensation reaction with 44.6% overall yield.
以蛋氨酸为原料经还原脱硫甲基化、酯化、氨解、酰胺化及分子内缩和成环4步反应合成得到了左乙拉西坦，总收率44.6%。
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