1)  Dodecylpyridinium bromide
溴代十二烷基吡啶
2)  bromination
溴代
1.
Study on synthesis bromination derivatives of polyethylene glycol monomethyl ether;
聚乙二醇单甲醚溴代衍生物的合成研究
2.
Comparing to different reaction methods, the method starting from 1,3-dimethyladamantane was certified with the memantine hydrochloride synthesized by bromination ,acetimidolation, hydrolysis and acidation.
通过比较不同的反应路线,确定了以1,3-二甲基金刚烷为原料,经溴代、乙酰氨基化、水解反应最后经酸化得到盐酸美金刚胺。
3.
Bromacil was synthesized using 2-bromobutane and urea as the starting materials in three steps including condensation,cyclization and bromination with total yield of 61%.
以2-溴丁烷和尿素作为起始原料,经缩合、环化、溴代三步反应得到除草定,总收率为61%。
3)  bromization
溴代
1.
The Study on Bromization of Benzene on the Platinum Electrode By Confocal Microprobe Raman Spectroscopy;
苯在铂电极上溴代反应的共焦显微拉曼光谱研究
4)  aryl bromide
溴代芳烃
1.
Suzuki cross-coupling reactions between aryl bromides and phenylboronic acids were studied over a hydroxyapatite-supported Mn catalyst(MnHAP) for the first time.
对于不同取代基取代的溴代芳烃或苯硼酸,可以得到中等产率(18%~46%)的偶联产物。
2.
The palladium catalyst supported on fluoride pillared layered double hydroxide(LDH-F) was prepared by the incipient wetness method,and it was used to catalyze the Heck and Suzuki coupling reactions of aryl bromides.
以氟离子插层的水滑石LDH-F为载体,用逐滴浸渍法制备了新型Pd/LDH-F催化剂,并用其催化溴代芳烃的Heck和Suzuki偶联反应。
5)  α-bromoketone
α-溴代酮
1.
6 were obtained from thioamides and α-bromoketones by a four-step reaction.
以硫代酰胺和α-溴代酮为原料,经4步反应合成了N,N′-二酰基肼(6),6在POCl3作用下脱水环化,合成了7个未见文献报道的2-芳基-5-[(4-芳基噻唑-2-基)甲基]-1,3,4-噁二唑类化合物,其结构经1H NMR,IR,MS和元素分析表征。
2.
Quinoxalines were obtained from α-bromoketones,1,2-diaminobenzene and DMSO in a solvent-free one-pot process at room temperature under grinding.
在室温无溶剂条件下,将α-溴代酮、邻苯二胺和二甲亚砜(DMSO)置于研钵中研磨,一锅法合成了一系列喹喔啉类化合物。
3.
On the basis of this, the additionreactions of N-sulfonylimines with α-bromoketones and α-bromoesters in the presentof zinc powder were carried out.
在此基础上又研究了α-溴代酮和α-溴代酯在金属锌的作用下与磺酰亚胺的加成反应。
6)  α-bromination
α-溴代
参考词条
补充资料:1-溴代十二烷
分子式:C12H25Br
分子量:249.24
CAS号:143-15-7

性质:无色至淡黄色液体。熔点-9.5℃,沸点276℃,200-201℃(13.3kPa),139℃(1.33kPa),134-135℃(0.8kPa),相对密度1.0399(20/4℃),折光率1.4583,闪点110℃。能与丙酮混溶,溶于乙醇,乙醚,不溶于水。有椰子样气味。有刺激性。

制备方法:1.氢溴酸法 由月桂醇(正十二醇)与氢溴酸作用而得。将月桂醇加入搪瓷玻璃反应锅,搅拌冷却,慢慢加入硫酸。搅拌1h,再加入氢溴酸。温度逐渐提高到90-95℃,搅拌反应8h。反应完毕,降温至30℃静置8h 。分出酸层,油层用稀碱液调节pH至8,分去碱液,以50%乙醇洗涤。减压蒸馏,收集140-200℃(3.33kPa)馏分得精制的1-溴十二烷。2.溴化钠法3.溴化法

用途:用作溶剂,还可用于合成阻燃剂三(十二烷基硫醇)锑、抗氧剂十二烷基硫醇、表面活性剂十二烷基二甲基苄基氯化氨(洁尔灭)、苯扎溴铵,以及其他阻燃剂和表面活性剂等。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。