丁二酰

It was found that SnCl_2·2H_2O is an effective catalyst for the acylation of 2,3-dimethyl-2-butene by acetic anhydride at room temperature.

发现SnCl2·2H2O是室温下2，3-二甲基-2-丁烯与乙酐进行酰化反应的有效催化剂。

It is broken down via phenylalanine to give acetyl CoA and fumaric acid.

它通过苯丙氨酸降解出乙酰辅酶 A 和反丁烯二酸。

To study the analysis method of samples including a combination of dimethylformamide, undecane and butanone in the air of workshop.

［目的］研究工作场所环境空气中二甲基甲酰胺、十一烷和丁酮混合物一次吸附、一次分离的定量分析方法。

Some materials were synthesized in this paper at first, 1-nitro-2-pentanol was synthesized with nitromathane and butyraldehyde and the yield was 70.2%; l-nitro-2-pentanol was reduced to 1 -amino-2- pentanol with iron and the yield was 65.2%.

分别用氢氧化钠、三乙胺为缚酸剂，2-氨基-1-丁醇、1-氨基-2-戊醇、环己酮和二氯乙酰氯为原料，采用一步法和分步法合成了两种潜在除草剂安全剂。

The invention provides a method to prepare 3, 3-dimethyl butyric acid chloride, which is simple in process, simple in operation and low in cost, with high safety and little pollution to the environment.

提供一种工艺简单、操作简便、安全性高、生产成本低、对环境影响小的3，3-二甲基丁酰氯的制备方法。

What's more, we measure the inhibition rate of calcium carbonate and conglutination of the polymaths.

以丙烯酸、顺丁烯二酸酐和丙烯酰胺为原料，过硫酸钾为引发剂，在不同的条件下进行自由基聚合反应，生成不同分子量的共聚物，并测定了这些共聚物的粘度和对碳酸钙的阻垢率。

Experimental process: jing and 3- methyl -2- methyl ethyl ketonesynthesizes by the benzene zong; Again the glacial acetic acidcatalysis produces 2, 3, 3 - trimethyl - 3H - yinduo; Again has thealkylate response production yinduo iodide after the methyl iodide;The iodide takes off molecular HI under NaOH to become freejier thealkali; Adds 5 - nitryls salicylic aldehydes in the ethyl alcohol forthe solvent under if to respond finally produces 6 '- the nitryl yinduolin spiral benzene and pinan; Through the infrared spectrum andthe ultimate analysis irrevocably proved its structure, and studiedthe annulus with to open the annulus the light to send changes colorthe performance, explained in different solvent medium ultravioletabsorption spectrometry solvent effect, and the comparisondiscoloration the response speed number difference, finally mixed itadds to the methyl methacrylate, the peroxidation benzoin formyl in the plexiglass, tested 6 '- the nitryl yinduolin spiralbenzene and pinan in the glass fatigue resistance, thethermostability.

实验过程：由苯肼和3-甲基-2-丁酮合成腙；再冰醋酸催化生成2 ，3 ，3—三甲基—3H—吲哚；再经过碘甲烷发生烷基化反应生成吲哚碘化物；碘化物在NaOH下脱去一分子HI成为费歇尔碱；在乙醇为溶剂下加5－硝基水杨醛与其反应最后生成6'—硝基吲哚啉螺苯并吡喃；通过红外光谱和元素分析确证其结构，并研究了环体与开环体的光致变色性能，解释了在不同溶剂介质中紫外吸收光谱的溶剂效应，并比较褪色反应速率数的差异，最后将其掺加到甲基丙烯酸甲酯，过氧化二苯甲酰有机玻璃中，测试6'—硝基吲哚啉螺苯并吡喃在玻璃中的抗疲劳性、热稳定性。

The same is carried out in the microwave, ethanol, dichloroethane, sodium carbonate, tetrabutylammonium iodide ammonium dissolved in dimethylformamide, then access to carbon dioxide.

同样是在微波炉中进行，把乙醇，氯乙烷，碳酸钠，四丁基碘化铵溶解在二甲基甲酰胺中，再通入二氧化碳。

Project Background and Conditions: The company started research new chemical products in 1998. After two years of efforts, a series of pharmaceutical intermediate sulfathiazole leave instructions, including : 3- methyl sulfathiazole leave instructions, 2- sulfathiazole leave instructions ethanoic acid, 2- acetyl sulfathiazole leave instructions, 2-thiofuran amino ethane ,2-thiofuran acetic, 3,4,5- tighter nitrobenzene have been successfully developed. 2-thiofuran amino ethane are the precursors raw materials of series antibiotic analgesic.

二、项目建设背景及条件：1998年公司开始研究开发高新精细化工产品，经过两年的努力，已成功研制出噻吩系列医药中间体，包括：3-甲基噻吩、2-噻吩乙酸、2-乙酰噻吩、2-噻吩乙胺、2-噻吩乙醇、3，4，5-三氯硝基苯等。2-噻吩乙胺系列噻吩产品使用于血小板及血栓有关的心脏血管病及消炎镇痛等如氯吡格雷、兴孢噻吩钠、兴孢西丁、噻吩洛酸等十几种新药的前体原料，是国家政策鼓励发展和有自主知识产权的项目。

Two compounds were synthesized with two methods. The two compounds can be synthesized by two steps with triethylamine as catalyst.

分别用氢氧化钠、三乙胺为缚酸剂，3-氨基-2-丁醇、2-氨基-3-戊醇、环己酮和二氯乙酰氯为原料，采用一步法和分步法合成了两种潜在除草剂安全剂。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。