1) bromcamphor
溴代樟脑
2) D-3-bromophor-8-sulfonic acid ammonium salt
D-3-溴代樟脑-8-磺酸铵
3) 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%。
4) 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
5) 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。
6) 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。
参考词条
补充资料：2-溴代异丁酰溴
分子式：C4H6Br2O
分子量：229.91
CAS号：20769-85-1
性质：带红色液体。沸点162-164℃，相对密度1.860，折光率1.5080。溶于卤代烃，遇水、醇分解。
制备方法：将溴滴加到异丁酸和红磷的混合物中，在100℃反应6h，减压蒸出未反应的溴和溴化氢。冷却，分去亚磷酸，得2-溴代异丁酰溴粗品。粗品经减压分馏，收集91-98℃（13.3kPa）馏分，即为成品。
用途：有机合成中间体。
分子量：229.91
CAS号：20769-85-1
性质：带红色液体。沸点162-164℃，相对密度1.860，折光率1.5080。溶于卤代烃，遇水、醇分解。
制备方法：将溴滴加到异丁酸和红磷的混合物中，在100℃反应6h，减压蒸出未反应的溴和溴化氢。冷却，分去亚磷酸，得2-溴代异丁酰溴粗品。粗品经减压分馏，收集91-98℃（13.3kPa）馏分，即为成品。
用途：有机合成中间体。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。