以对三氟甲基苯胺为原料,经重氮化、肟化、水解制得对三氟甲基苯甲醛,收率35。
The starting reagent, p-trifluoromethylaniline, was subjected to diazotization, oximation, and hydrolyzationto synthesize p-trifluoromethyl benzaldehyde, with a total yield of 35.
方法:以3-三氟甲基- 4-氰基苯胺和2- 甲基丙烯酰氯为起始原料经过酰化、 环氧化、取代和氧化四步反应合成比卡鲁胺。
Methods:Bicalutamide was prepared from 4-cyano-3-(trifluoromethyl) aniline and 2-methylacryloyl chloride by four steps: acylation, cyclization, substitution, and oxidization.
然后研究了三氟甲磺酸镱催化的胺和乙酸乙酯的反应,从而合成了乙酰苯胺类化合物。
Objective:To study the anti tumor effects of Sorbaria sorbifolia ethyl acetate extract and its mechanism.
本文以邻甲基苯胺、对氯苯胺、间三氟甲基苯胺和5-三氟甲基-1,3-苯二胺为单体,利用电化学方法,得到了上述苯胺衍生物的聚合物薄膜。
In this paper, polymer films were prepared with o-toluidine, p-chloroaniline, m-trifluoro methylaniline and 5-trifluoromethyl-1,3-diaminobenzene as monomer by electrochemical method.
以邻三氟甲基苯胺为起始原料,二水氯化铜为催化剂,盐酸-双氧水为氯化剂,合成4 -氯- 2 -三氟甲基苯胺。
4-chloro-2-trifluoromethyl aniline was synthesized from 2-trifluoromethyl aniline, using hydrochloric acid-hydrogen peroxide as the chlorination agent and cupric chloride as the catalyst.
通过近年某些国家对来氟米特副作用的论证,分析了可能对来氟米特的应用市场造成一定的影响,进而影响其中间体5 甲基异唑4 甲酰氯和对三氟甲基苯胺的市场。
Through the demonstration on side-effect of leflunomide made by some countries recently, the probable impact to application market of leflunomide and to its intermediates could be given.
通过近年某些国家对来氟米特副作用的论证,分析了可能对来氟米特的应用市场造成一定的影响,进而影响其中间体5 甲基异唑4 甲酰氯和对三氟甲基苯胺的市场。
Through the demonstration on side-effect of leflunomide made by some countries recently, the probable impact to application market of leflunomide and to its intermediates could be given.
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