Dong, Jinhuan; Xin, Shuang; Wang, Yanqing; Pan, Ling; Liu, Qun published an article in 2017, the title of the article was In situ generation and reactions of p-(trifluoromethyl)benzyl electrophiles: an efficient access to p-(trifluoromethyl)benzyl compounds.Recommanded Product: 1-Fluoro-2-methoxybenzene And the article contains the following content:
A new three-component reaction, namely condensation-anti-Michael addition-aromatization, enabling the construction of benzylic compounds was disclosed. This reaction not only acted as an alternative approach to regioselective Csp2-H trifluoromethylation of arenes through an “aromatic to be” strategy, but also provided a simple, convenient, step-economic and practical strategy for the in-situ generation of electrophilic p-(trifluoromethyl)benzyl species under extremely mild conditions. The experimental process involved the reaction of 1-Fluoro-2-methoxybenzene(cas: 321-28-8).Recommanded Product: 1-Fluoro-2-methoxybenzene
The Article related to trifluoromethyl trimethylsilyloxycyclohexadienone ketone sulfonamide indium triflate catalyst tandem reaction, trifluoromethylbenzylamine regioselective preparation arene, methane diaryl preparation regioselective, arene trifluoromethyl trimethylsilyloxycyclohexadienone ketone indium triflate catalyst tandem reaction, diarylmethane preparation regioselective and other aspects.Recommanded Product: 1-Fluoro-2-methoxybenzene
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