二溴乙烷

In this paper,the advantages of a new type of bromine flame retardant decabromodiphenylethane are introduced.

介绍了新型高效溴系阻燃剂十溴二苯乙烷的突出优点，介绍了我国十溴二苯乙烷的生产方法和现状，讨论了国内十溴二苯乙烷的研究及应用研究情况，展望了十溴二苯乙烷的发展前景。

Bis(1,2,3,4-tetrahydroisoquinoline-2-ylmethyl) HBr salt (K2) guest has been synthesized from 1,2,3,4- tetrahydroisoquinoline and ethylenedibromide. The self-assembly interaction models of cucurbit[8]uril (Q[8]) with this synthetic guest have been investigated by using 1H NMR technique, single crystal X-ray diffraction determination and theoretic calculation method.

以用1，2，3，4-四氢喹啉和二溴乙烷合成的二(2-亚甲基-1，2，3，4-四氢异喹啉)的溴化氢酸盐为客体，八元瓜环为主体，利用1H NMR技术，单晶X射线衍射方法以及理论计算等方法，考察了两者的自组装模式。

According to concerned papers ,we have chosen the way in which diquat dibromide is synthesized from 2,2-bipyridyls and ethylene dibromide. This paper makes further research into its technology, thus obtaining better synthesizing conditions.

本文在查阅大量文献的基础上，采用以2，2'-联吡啶和1，2-二溴乙烷为原料合成敌草快二溴盐的合成路线，并对其合成工艺进行了深入的研究，筛选出较佳的工艺条件。

Two kinds of di aniline derivative s connected with oxamethylene bridge or azamethylene bridge were synthesizied by condensation of o nitrophenol and ethylene dibromide (1,4 dibromobutane)or 4 chloro 3,5 dinitrobenzotyifluoride and ethylene diamine(1,6 hexandiamine)and consequent reduction.

由邻硝基苯酚和二溴乙烷以及由4－氯－3， 5－二硝基三氟甲苯和乙二胺为原料通过桥接、还原合成两类由氧亚甲基或氮亚甲基桥联的双苯胺衍生物。

A better understanding of the role of PPAR in insulin action system will be critical in developing more efficacious and safe agent s that act on PPAR and benefit patients with type 2 diabetes. The main content is followed: Synthesis and analysis of 1,3-dicarbonyl compounds. Make use of easily available cheap reagent such as 2-naphthol, 6-hydroxyquinoline, 1,2-dibromoethane, 4- hydroxybenzaldehyde, dimethyl malonate, 2-{4- [(2-napthoxy)ethoxyl] benzyl} malonates and 2-{4 [(1,2,3,4-tetrahydro-6 -quinolinoxy)ethoxyl] benzyl } malonates were synthesized through 6-8 steps in virtue of Williamson, Knoevenagel reaction, Pd/C catalyzed hydrogenation with mild conditions and high yield. The total yield of 40-50%.

本论文的主要内容和研究结果如下： 1，3-二羰基类化合物的合成及分析，采用2-萘酚、6-羟基喹啉、1 ，2二溴乙烷、对羟基苯甲醛、丙二酸二甲酯等常见易得试剂，利用Williamson反应、Knoevenagel反应、钯碳加氢等条件温和且收率高的方法，分别合成了2-{4- [(2-萘氧)乙氧基]苄基}丙二酸衍生物和2-{4 [(1，2，3，4-四氢-6-喹啉氧基)乙氧基]苄基}丙二酸衍生物两个系列8个化合物，经6-8步反应，总收率为40-50%，具有一定绿色化学特性。

The experimental result showed that three byproducts was formed and the optimal condition was as follows: the molar ratio of ethylene glycol, hydrogen bromide, and acetic acid was 1:1:1.3, when ethylene glycol was 1 mol, refluxed 5 h under the action of 100 mL toluene.

结果表明：较适宜的合成条件为乙二醇1 mol， n：n：n=1：1：1.3，在带水剂甲苯(100 mL)的作用下，回流反应5 h，约4 h后分两次追加0.12×2 mol醋酸酐，合成效果最好，产率可达到95%，反应副产2-溴乙醇及少量的1， 2-二溴乙烷、乙二醇二乙酸酯和二乙二醇二乙酸酯。

This investigation focuses on pigment phthalocynine green G modified with octadcylamine, which is suspended in tetrachloroethylene and 1,2-dibromoethane using span-80 and CH-6 hyperdispersants as emulsifiers.

采用正交设计方法，以十八胺改性酞菁绿G形成电泳颗粒，以四氯乙烯和1，2-二溴乙烷的复配液为分散介质，Span-80和CH-6超分散剂为稳定剂，制备了分散性和稳定性良好的电泳显示液。

Bis-imidazoline was prepared from triethylene tetraamine and N,N-dimethylformamide dimethyl acetal at 85℃ for 2 h with toluene as solvent, with a yield of 90.4%. The reaction of bis-imidazoline with 1,2-dibromoethane and potassium carbonate in acetonitrile provided with a monobromide salt yield of 78.7%. Hydrolysis of monobromide salt under aqueous causic solution formed 1,4,7,10-tetraazzcyclododecane in a 74.2% yield.

用甲苯作溶剂，使三乙烯四胺和N，N-二甲基甲酰胺二甲基缩醛在85℃反应2 h，得到中间体双咪唑啉，产率90.4%，在乙腈溶剂中，碳酸钾存在下，双咪唑啉和1，2-二溴乙烷进行扩环反应，得到环状中间体一溴盐，产率78.7%，一溴盐经碱性水解2 h，得到1，4，7，10-四氮杂十二烷，产率74.2%。

Deoxybenzoin(3) was prepareded by using the resorcinol and substituted phenylacetic as starting meterials in microwave-mediated.Then the compound(3) was reacted with acetic anhydride to produce(4).The compound(4) was hydrolyzed to convert compound(5) in the acid-mediated. The compound(5) was reacted with the 1,2-dibromo-ethane and 1,3-dibromo-propane in refluxed condition with acetone as solvent to give(6) or(7),respectively.Lastly,the title compounds were synthesized by refluxing(6) or(7) with 2-methyl-benzimidazole and potassium carbonate in acetone solution.

以取代苯乙酸和间苯二酚为起始原料，用微波辐射法合成脱氧安息香(3)，(3)与乙酸酐缩合生成2-甲基-7-乙酰氧基异黄酮(4)，(4)在酸性条件下水解生成相应的异黄酮(5)，化合物(5)分别与1，2-二溴乙烷和1，3-二溴丙烷反应生成(6)和(7)，化合物(6)和(7)再分别与2-甲基苯并咪唑偶合生成目标化合物。

In this thesis, the design, synthesis and application of substituted 1,8-naphthalimides and napthopyrones conjugated with uridine, substituted 1,3,5-triazine, 1,2-dibromoethane, ethyl bromoacetate have been studied.

本论文研究了取代l，8-萘酰亚胺和萘并吡喃酮与尿苷、取代均三嗪、二溴乙烷、溴乙酸乙酯偶合和双l，8-萘酰亚胺之间偶合的设计、合成及应用。

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。