查询词典 benzoyl-glycine

A synthesis method of 2-(2'-hydroxyl-4'-benzoyloxy-phenyl)-2H-benzotriazole and derivatives thereof is provided, and is characterized in that 2-(2', 4'-dihydroxyphenyl)-5-X-2H-benzotriazole and benzoyl chloride are taken as raw materials for reaction in solvent for 1-8 hours under the temperature of 50-140 DEC C with the mole ratio of 1 to 0.95-1.1, wherein, the amount of the solvent is 2 to 20 times that of the 2-(2', 4'-dihydroxyphenyl)-5-X-2H-benzotriazole and X represents H, F, Cl, Br.

一种2-(2′-羟基-4′-苯甲酸基苯基)-2H-苯并三唑及其衍生物的合成方法，其特征是，以2-(2′，4′-二羟基苯基)-5-X-2H-苯并三唑和苯甲酰氯为原料，在溶剂中进行反应，反应温度50℃～140℃，反应时间1～8小时，反应原料摩尔比2-(2′，4′-二羟基苯基)-5-X-2H-苯并三唑∶苯甲酰氯为1∶0.95～1.1，溶剂用量为2-(2′，4′-二羟基苯基)-5-X-2H-苯并三唑重量的2～20倍，其中X代表H、F、Cl、Br，具有反应条件温和、反应收率高和产物纯度高的特点。

The thermokintics of nucleophilic substitution reactionsof benzoyl chloride and oxidation reaction of isopropanol by NBS have been studiedby using the mathematical models of the thermokinetic time-parameter method forsimple and consecutive first order reaction, respectively. The kinetic mechanisms ofstudied reactions have been discussed reasonably.

利用简单和连续一级反应的时间参量法的数学模型，分别研究了苯甲酰氯亲核取代反应和NBS氧化异丙醇反应的热动力学，对反应的机理进行了合理的解释和讨论。

The effect of reaction temperature,reaction time,materials ratio on the synthesis of piperidine alcohol benzoate ,hindered amine light stabilizer,from piperidine alcohol and benzoyl chloride by direct condensation were studied,and the proper technological conditions were given as follows:the reaction temperature is 95℃;reaction time is 4 h; the mole ratio of reactants,n∶n is 1∶1.4,the amounts of solvent is 40 mL(based 0.1mol piperidine alcohol),the arerage yield ...

王树清，高崇，苯甲酸哌啶醇酯HALS的合成工艺研究研究了以苯甲酰氯和哌啶醇为原料直接缩合合成苯甲酸哌啶醇酯受阻胺光稳定剂时反应温度、反应时间、原料配比等条件对合成反应的影响，确定了最佳工艺条件。最适宜的工艺条件是：反应温度95℃、反应时间6h、原料摩尔比n∶n为1∶1.4，溶剂用量为70mL(相对于0.1mol哌啶醇)，苯甲酸哌啶醇酯的收率为91.05%，产品纯度98.5%。

The "one-pot" synthetic reaction of 2-alkylthio-4-amino-5-cyano-6-methylthiopyrimidines from bis(methylthi-o)methylene propanedinitrile was perfected and the average yield was increased to above 70% in the present of KF/Al2O3 The problem that the amino group of above mention- ed pyrimidine compounds were hard to be acylated by trichloroacetyl chloride and benzoyl chloride was resolved by the use of NaH.

在研究合成方法的过程中，论文对KF/Al2O3催化合成本文嘧啶化合物4的&一锅煮&方法进行了完善和改进，扩大了&一锅煮&法的应用范围，可以直接使用硫酸酯、卤代烷、对甲苯磺酸酯进行合成，平均产率达到70%以上。

Seven biogenic amines were extracted from a sample with 6% perchloric acid, then derivatized with benzoyl chloride. 0.02 mol/L borate buffer (pH 9.2) containing 0.06 mol/L sodium deoxycholate-methanol （95∶5, v/v）was used as a running buffer. The detection wavelength was set at 214 nm. The separation was achieved within 12 min. Good linearities were observed from the calibration plots in the concentration ranges.

样品经6%过氯酸萃取后，由苯甲酰氯衍生化，以含0.06 mol/L脱氧胆酸钠的0.02 mol/L硼酸(pH 9.2)-甲醇(体积比为95∶5)混合液为电泳介质，电泳电压25 kV，温度25 ℃，检测波长214 nm，在12 min内实现了7种生物胺的完全分离。7种生物胺的浓度与其峰面积在一定的范围呈良好的线性关系，检出限除组胺为15 μg/g外，其余均为5 μg/g。

Methyl phenyl glyoxylate was prepared firstly by reaction of 2-methyl benzoyl chloride with NaCN. The reaction of 2-methyl phenyl glyoxylate with methanol gave the target product methyl 2-methyl phenyl glyoxylate. An improved 3 step synthetic method of methyl 2-methyl phenyl glyoxylate was studied. The optimization conditions were presented.

以2-甲基苯甲酸为原料，酰化后与氰化钠反应生成2-甲基苯甲酰腈，经甲酯化生成2-甲基苯甲酰甲酸甲酯，改进了三步合成2-甲基苯甲酰甲酸甲酯的方法，并对反应时间、反应温度等影响因素进行了优化，确定了合成反应中的最优化条件。

Nine sugars and five sugar alcohols were analysed by HPLC with a differenctial refractometerdetector. p-Methoxyaniline and benzoyl chloride were used to the pre-column derivatization of sugar and sugar alcohol, in which a ultraviolet absorption organic group was added, Then the derivatives were detected sensitively by an UV monitor sensitively.

采用高效液相色谱示差折光检测器，对9种糖和五种糖醇进行了分离检测；另以对甲氧基苯胺和苯甲酰氯为衍生试剂，分别对糖和糖醇进行柱前衍生，使其接上紫外吸收基团，然后用紫外检测器进行检测。

First, by using p-methoxybenzaldehyde , p-hydroxybenzaldehyde and pyrrole as raw materials, 5-(p-hydroxyphenyl)-10,15,20-tri(p-methoxyphyenyl)porpyrin was prepares under acidity condition and the let reacted with benzoyl chloride, o-nitrobenzoyl chloride, m- nitrobenzoyl chloride and p- nitrobenzoyl chloride respectively under alkalinity condition with DMF as solvent.

以对-甲氧基苯甲醛、对-羟基苯甲醛和吡咯为原料，在酸性条件下合成了5-对羟苯基10，15，20-三对甲氧苯基卟啉，再以该化合物为原料分别与苯甲酰氯、邻-硝基苯甲酰氯、间-硝基苯甲酰氯和对-硝基苯甲酰氯反应，在碱性条件下以DMF为溶剂合成了四种目前尚未见文献报道的对-甲氧基卟啉硝基苯甲酸酯类化合物。

The optimal operation condition of Friedel-Crafts acylation for product Ⅰ was determined by orthogonal experiment: 0.02mol N-ethyl- carbazol, n Benzoyl chloride/n N-ethyl- carbazol=1.2, n AlCl3/n N-ethyl- carbazol=1.2 , at 25 oC for 3.5h. The yield was 94.6%.

通过正交设计实验，探讨了产物Ⅰ的Friedel-Crafts 酰化的最佳反应条件：N-乙基咔唑为0.02mol时，反应物苯甲酰氯与N-乙基咔唑摩尔配比为1.2。，催化剂AlCl3与N-乙基咔唑摩尔配比为1.2， 25℃下反应3.5h，产率可达94.6%。

Synthesis and structural characterization of novel cycioplatinated complexes with 2-aryl imidazolines 2-arylimidazoline ligands 2a-2d were synthesized from benzoyl chloride or p-methoxybenzoyl chloride with aminoethanol or valinol and 2e was synthesized from 2-phenylimidazoline.

新型2-芳基咪唑啉环铂化合物的合成与结构表征以苯甲酰氯或4-甲氧基苯甲酰氯和氨基醇(2-氨基乙醇或外消旋的缬氨基醇)为原料，合成了四种2-芳基咪唑啉配体2a-2d，以2-苯基咪唑啉为原料合成了配体2e，其中2d为新化合物。

But we don't care about Battlegrounds.

但我们并不在乎沙场中的显露。

Ah! don't mention it, the butcher's shop is a horror.

啊！不用提了。提到肉，真是糟透了。