Method for catalytically depolymerizing lignin by using MTO (Methyltrioxorhenium) under microwave promoted condition
A technology of methyl rhenium trioxide and catalytic depolymerization, applied in chemical instruments and methods, preparation of carbon-based compounds, preparation of organic compounds, etc., can solve the problems of consuming large external hydrogen sources, destroying benzene rings, increasing costs, etc. , to achieve high atom economy, fast reaction speed and high selectivity
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[0020] Preparation of ionic liquid solvent: refer to literature (C.P.Fredlake, J.M.Crosthwaite, D.G.Hert, S.N.U.K.Aki, J.F.Brennecke, J.Chem.Eng.Data, 2004, 49, 954.; Webb P B, Sellin M F, Kunen T E, et al.J .Am.Chem.Soc.2003,125,15577.) Prepared and purified dozens of ionic liquids with strong dissolving ability of lignin, which are used for the implementation of the patent of the present invention.
[0021] Methyl rhenium trioxide catalyzes the depolymerization of lignin model compounds and organic lignin under microwave conditions, including
[0022] Include the following steps:
[0023] ① Lignin model compound or organic lignin and catalyst are preheated and dissolved in ionic liquid at 80°C to 120°C;
[0024] ②Transfer the aforementioned mixture to a microwave reaction system and react under microwave radiation conditions. The rated power used for microwave radiation is 240W, and the reaction time is 2 minutes;
[0025] ③ after the reaction finishes, extract the reactio...
Embodiment 1
[0028] 1 gram of ionic liquid 1-butyl-3-methylimidazole bistrifluoromethylsulfonimide [C 4 MIm]NTf 2, 50 mg lignin model compound β-O-4: 2-(2-methoxyphenoxy)-1-phenylethanol, and 2.5 mg catalyst methyl rhenium trioxide were heated to 80 ℃, fully dissolved; transfer the liquid material to a microwave reaction system, and react under microwave radiation (power 240W) for 2 minutes; cool the reaction mixture to room temperature, dilute to 25 ml with a solution of acetonitrile: water 6:4 , into the liquid chromatography analysis, the conversion rate is 98%, the yield of guaiacol is 69%, and the yield of phenylacetaldehyde is 64%.
Embodiment 2-3
[0030] Other process conditions and experimental steps are the same as in Example 1, but using different reaction times, the results are shown in Table 1.
[0031] Table 1. Depolymerization of lignin model compounds under different reaction time conditions
[0032]
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