Zhang, JJ; Qian, QL; Wang, Y; Bediako, BBA; Yan, J; Han, BX in [Zhang, Jingjing; Qian, Qingli; Wang, Ying; Bediako, Bernard Baffour Asare; Yan, Jiang; Han, Buxing] Chinese Acad Sci, CAS Key Lab Colloid Interface & Chem Thermodynam, CAS Res Educ Ctr Excellence Mol Sci, Beijing Natl Lab Mol Sci,Inst Chem, Beijing 100190, Peoples R China; [Zhang, Jingjing; Wang, Ying; Bediako, Bernard Baffour Asare; Yan, Jiang; Han, Buxing] Univ Chinese Acad Sci, Sch Chem & Chem Engn, Beijing 100049, Peoples R China; [Qian, Qingli; Han, Buxing] Huairou Natl Comprehens Sci Ctr, Phys Sci Lab, 5 Yanqi East Second St, Beijing 101400, Peoples R China; [Han, Buxing] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China published Synthesis of ethanol from aryl methyl ether/lignin, CO2 and H-2 in 2019, Cited 42. Product Details of 98-17-9. The Name is 3-(Trifluoromethyl)phenol. Through research, I have a further understanding and discovery of 98-17-9.
Currently, ethanol is produced via hydration of ethene or fermentation of foods. Lignin and CO2 are abundant, cheap and renewable feedstocks. Synthesis of ethanol using the lignin or its derivatives is of great importance, but is a great challenge and has rarely been reported. Herein, we propose a route to synthesize ethanol from CO2, H-2, and lignin or various aryl methyl ethers, which can be derived from lignin. The reaction could be effectively conducted using Ru-Co bimetallic catalyst and the TON of ethanol could reach 145. Interestingly, ethanol was the only liquid product when lignin was used. A series of control experiments indicate that ethanol was formed via cleavage of aryl ether bond, reverse water gas shift (RWGS) reaction, and C-C bond formation. This protocol opens a way to produce ethanol using abundant renewable resources.
About 3-(Trifluoromethyl)phenol, If you have any questions, you can contact Zhang, JJ; Qian, QL; Wang, Y; Bediako, BBA; Yan, J; Han, BX or concate me.. Product Details of 98-17-9
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
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