Safety of Benzyl ether. Authors Liu, L; Tang, YY; Wang, KY; Huang, TZ; Chen, TQ in AMER CHEMICAL SOC published article about in [Liu, Long; Tang, Yuanyuan; Wang, Kunyu; Huang, Tianzeng; Chen, Tieqiao] Hainan Univ, Hainan Prov Fine Chem Engn Res Ctr, Hainan Prov Key Lab Fine Chem, Key Lab,Minist Educ Adv Mat Trop Isl Resources, Haikou 570228, Hainan, Peoples R China in 2021, Cited 73. The Name is Benzyl ether. Through research, I have a further understanding and discovery of 103-50-4
A facile and general method for constructing carbon-heteroatom (C-P, C-O, C-S, and C-N) bonds via C-N cleavage of benzyl ammonium salts under transition-metal-free conditions was reported. The combination of t-BuOK and 18-crown-6 enabled a wide range of substituted benzyl ammonium salts to couple readily with different kinds of heteroatom nucleophiles, i.e. hydrogen phosphoryl compounds, alcohols, thiols, and amines. Good functional group tolerance was demonstrated. The scale-up reaction and one-pot synthesis were also successfully performed.
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Reference:
Ether – Wikipedia,
,Ether | (C2H5)2O – PubChem