• 结论产物首次得到。

    Conclusion the product was obtained for the first time.

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  • 目的研究头孢呋辛氨解机理产物

    Objective To study the mechanism of aminolysis and degradation product of cefuroxime sodium.

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  • 探讨过渡金属麦草碱木质素过氧化氢氧化影响。

    The effects of transitional metal ions on the oxiammonolysis of wheat straw alkaline lignin with hydroperoxide were studied.

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  • 麦草木质素木材硫酸盐木质素氧化反应进行研究。

    Oxidative ammonolysis reaction of wheat soda lignin and wood kraft lignin was studied.

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  • 研究麦草木质素过氧化氢氧化氨解主要官能团影响

    The effects of oxiammonolyzation by hydroperoxide on the main functional groups of wheat straw alkaline lignin were studied.

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  • 方法以辛二起始原料缩合、活化氨解合成SAHA

    Methods: Suberic acid was selected as the start material, and the SAHA was obtained through condensation, activation and ammoniated.

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  • 吡咯烷酮经N烷基化氨解反应合成了乙拉西坦,收率42.6%。

    Etiracetam was synthesized from 2-pyrrolidone by N-alkylation and aminolysis. The overall yield was 42.6%.

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  • 利用磷肥产氟硅酸原料,采用作为制备补强炭黑

    High reinforced white carbon black is prepared by using phosphate fertilizer's by-product fluosilicic acid as raw material and ammonia water as ammonia analytical agent.

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  • 一般来说杂环化合物反应反应反应容易发生。

    It is generally noted that hydrolysis or alcoholysis of phosphorus heterocycles are favoured over aminolysis.

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  • 吲哚-3-乙酸催化氢化甲酯化氨解反应得到吲哚瞒-3-乙酰胺9);

    Firstly, indoline - 3 - acetamide ( 9) was prepared from indole - 3 - acetic acid by catalytic hydrogenation, esterification and aminolysis.

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  • 稻草硫酸铵法制废液采用氧化方法,将废液中的铵态转化有机氮。

    The nitrogen, which is in ammonium in the ammonia sulfite pulping waste liquor of rice straw, is converted into organic nitrogen by using oxide-ammonium decomposition method.

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  • 方法:以对硝基苯甲酰为原料,氨解氢化、重氮化及偶合反应得到了巴柳氮。

    METHODS:This compound was synthesize by steps of ammonolysis, hydrogenize, diazotization and coupling from 4 nitrobenzoyl chloride.

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  • 筛选2-丁酸起始原料氨解酯化拆分,环合五步反应得左乙拉西坦

    Screening for 2 - bromo- butyric acid as the starting material, after ammonolysis, esterification, ester amine solution, split, five-step cyclization reaction Levetiracetam.

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  • 筛选2-代丁酸起始原料氨解酯化拆分,环合五步反应得左乙拉西坦

    Screening for 2 - bromo-butyric acid as the starting material, after ammonolysis, esterification, ester amine solution, split, five-step cyclization reaction Levetiracetam.

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  • 讨论了以草酸二乙酯为原料,经过克莱森缩合、环合、氨解反应合成5甲基异唑3甲酰胺工艺改进

    This paper reports the improvement on the synthesis of 5 methylisoxazol 3 formamide by Claisen condensation of diethyl oxalacetate followed by cyclization and ammonolysis.

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  • 通过肥料沙柱淋溶性试验研究了以亚法制浆蒸煮废液氨解产物原料研制木质素肥料的缓释特性

    Through the leaching experiment, this paper studied on the slowly releasing characteristics of lignin compound fertilizer which was made of ammonia products of ammonia sulfite pulp black liquid.

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  • 环氧乙烷目前生产乙醇主要方法产品比例、产品质量能耗是乙醇胺生产中的三个关键因素

    Ethanolamines are commonly made by the method of reacting aqueous ammonia and ethylene oxide. Product profile, product quality and energy consumption are three key factors in ethanolamine process.

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  • 方法以1,4-丁烯二醇为原料,经过酯化环氧化、氨解开环四碘对苯二甲酰反应合成目标产物。

    METHODS The title compound was synthesized from 2-butene-1,4-diol, via esterification, epoxidation, amination, then amidation with tetraiodoterebenzoyl chloride.

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  • 所述组合含有溶剂代 硅化合物或者两种多种组合通过氨解作用得到的聚 硅氮烷化合物

    The composition contains a solvent and a polysilazane compound obtained by co-ammonolysis of one or a combination of two or more halosilane compounds.

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  • 综述2,6二甲基苯胺合成研究进展,对硝化还原法、甲基法、氨解法等合成路线及其所用催化剂进行了介绍

    The research progress in synthesis of 2, 6dimethylaniline was reviewed, and the catalysts used in various synthetic routes were introduced.

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  • 通过对对羟基扁桃氨解反应有关影响因素的研究,改进了氨解反应的条件,提高了反应收率,其工业化生产提供了依据

    The synthesis ofp-hydroxyphenylglycine is studied under different conditions. The overall yield is 92% and this method provided basis for industrialization.

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  • 为原料还原脱硫甲基化、酯化氨解酰胺化分子内缩成环4步反应合成得到了左乙拉西坦,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.

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  • 为原料还原脱硫甲基化、酯化氨解酰胺化分子内缩成环4步反应合成得到了左乙拉西坦,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.

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