A kind of preparation method of organic-inorganic hybrid material supporting ruthenium catalyst for synthesizing 1-aminopropanol
A hybrid material, ruthenium catalyst technology, applied in the preparation of organic compounds, the preparation of aminohydroxy compounds, organic compounds/hydrides/coordination complex catalysts, etc., can solve the problem of low yield, high cost, large catalyst consumption, etc. problem, to achieve the effect of high activity, low cost and high yield
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Embodiment 1
[0016] The present embodiment prepares catalyst sample 1 as follows:
[0017] a. Pretreat the silica gel to obtain spare silica gel
[0018] Add 10g of 100-200 mesh silica gel H, 120mL of 98% concentrated sulfuric acid and 15mL of 69% concentrated nitric acid into flask A, and stir in an oil bath at 140°C for 24 hours. Wash the silica gel H several times until the washing liquid is neutral, filter it with suction, take the solid intermediate A, wash the solid intermediate A with ethanol, and then put the filter cake in a vacuum drying oven at 140°C after suction filtration. Conditioned drying for 6 hours to obtain spare silica gel;
[0019] b. Grafting modified ethylenediamine structural units on the surface of spare silica gel
[0020] Add 60 mL of absolute anhydrous toluene and 1.4 g of N-(3-triethoxysilylpropyl) ethylenediamine to flask B, stir at room temperature for 30 min, then add 4 g of the spare silica gel obtained in step a, and stir until The spare silica gel is ...
Embodiment 2
[0024] This embodiment prepares catalyst sample 2 in the same manner as in Example 1, and changes the quality of N-(3-triethoxysilylpropyl) ethylenediamine into 1.8g in step b, and the obtained in step b The spare silica gel modified with ethylenediamine structural units on the surface has a mass percentage of nitrogen of 2.62% as measured by elemental analysis.
Embodiment 3
[0026] The present embodiment prepares catalyst sample 3 as follows:
[0027] a. Pretreat the silica gel to obtain spare silica gel
[0028] Add 10g of 100-200 mesh silica gel H, 120mL of 98% concentrated sulfuric acid and 15mL of 69% concentrated nitric acid into flask A, and stir in an oil bath at 100°C for 24 hours. Wash the silica gel H several times until the washing liquid is neutral, and filter with suction to obtain the solid intermediate A, wash the solid intermediate A with ethanol, and then place the filter cake in a vacuum drying oven at 140°C after suction filtration. Dry for 7 hours to obtain spare silica gel;
[0029] b. Grafting modified ethylenediamine structural units on the surface of spare silica gel
[0030] Add 80 mL of absolute anhydrous toluene and 1.4 g of N-(3-triethoxysilylpropyl) ethylenediamine to flask B, stir at room temperature for 30 min, then add 4 g of the spare silica gel obtained in step a, and stir until The spare silica gel is uniforml...
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