Catalyst for synthesizing methanol or its precursor, method for preparing catalyst and method for producing methanol or its precursor using catalyst
A technology for synthesizing methanol and catalysts, applied in organic compound/hydride/coordination complex catalysts, chemical instruments and methods, physical/chemical process catalysts, etc., can solve problems such as low selectivity, achieve good catalytic activity, and not easily Loss and decomposition, ensuring the effect of long-term use
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[0054] Another aspect of the present invention relates to a method for the preparation of a catalyst comprising reacting a substituted or unsubstituted aniline with a Pt salt, as shown in the following reaction scheme:
[0055]
[0056] Another aspect of the present invention relates to a method for methane oxidation comprising (a) contacting a catalyst for synthesizing methanol or a precursor thereof according to any embodiment with methane in the presence of an acid.
[0057] As previously mentioned, the catalyst for synthesizing methanol or its precursor represented by one of Formulas 1 to 3 according to the present invention may be used to form methyl ester through esterification to realize methane oxidation. The methyl esters can be used to form functional derivatives by subsequent reaction with nucleophiles.
[0058] Specifically, methyl esters can react with water as a nucleophile to synthesize methanol as a functional derivative. Methyl esters can also be reacted w...
Embodiment 1
[0079] Embodiment 1: the synthesis of catalyst compound
[0080] (1) Synthesis of compound 1-1
[0081] Bis(aniline)dichloroplatinum
[0082]
[0083] Will K 2 PtCl 4 (415 mg, 1.0 mmol) was added to an aqueous solution of aniline (502 mg, 5.4 mmol). After stirring well at room temperature for 18 hours, the precipitate was collected by filtration and washed with water and diethyl ether. The resulting solid was dissolved in dimethylformamide (DMF). The solution was stirred at 80°C for 3 hours. The reaction solution was concentrated under reduced pressure and precipitated with ether. The precipitate was collected by filtration to give the desired product (105 mg, 4.0 mmol) in 23% yield. 1 H NMR (400MHz, DMSO-d 6 )δ7.24-7.20 (m, 8H), 7.12-7.08 (m, 2H), 6.96 (s, 4H) (see image 3 )
[0084] (2) Synthesis of compound 1-2
[0085] Dichlorobis(4-methylaniline)platinum
[0086]
[0087] The desired product was obtained in a yield of 37% in the same manner as compoun...
Embodiment 2
[0132] Example 2: Synthesis of Methanol Precursor and Methanol
[0133] (1) Synthesis of methyl hydrogen sulfate
[0134] 1mg (2.6×10 -3 mmol) catalyst (dichloro-(N,N,N,N-tetramethylethylenediamine) platinum) represented by formula 3-2 and 30g containing 20% by weight SO 3 The oleum was mixed in a glass lined 100ml Inconel autoclave. The reactor was filled with methane gas to a pressure of 20 bar. The methane-filled reactor was heated to 180°C and the reaction was allowed to proceed for 3 hours. The pressure of methane at 180° C. was 35 bar at the initial stage of the reaction and decreased to 30 bar after 3 hours of reaction. After the reaction is complete, use a solution containing methanesulfonic acid (CH 3 SO 3 H) D as internal standard 2 SO 4 pass 1 H-NMR spectroscopy determines the structure of the product (see figure 1 ).
[0135] figure 1 Production of 1.89 g (16.9 mmol) of methyl hydrogensulfate was confirmed. The turnover number (TON) and turnover fr...
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