Organic bismuth ion compound containing bridge sulphur atom ligand, preparation and uses thereof
An ionic compound and organic bismuth technology, applied in the field of organic bismuth ionic compounds and their preparation, can solve problems such as weak acidity, and achieve the effects of simple preparation, wide application prospect, high catalytic activity and selectivity
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preparation example 1
[0036] Add 0.05mmol organic bismuth ion compound (R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 = H, X = OSO 2 C 8 f 17 ) and 2.0mL ethanol, 1.0mmol benzaldehyde and 1.0mmol aniline, after stirring for 5 minutes, 1.0mmol cyclohexanone was added, placed in a water bath reactor with magnetic stirring, and the reaction was carried out at room temperature at 25°C for 3 hours. TLC followed the reaction until the reaction was complete. The reaction result is: 2-(phenyl(anilino)methyl)cyclohexanone, the yield is 100%, and the selectivity of 2-(phenyl(anilino)methyl)cyclohexanone is 100%.
preparation example 2
[0038] Add 0.05mmol organic bismuth ion compound (R 1 , R 2 , R 3 , R 4 =CH 3 , R 5 , R 6 , R 7 , R 8 = H, X = OSO 2 C 4 f 9 ) and 2.0mL ethanol, 1.0mmol benzaldehyde and 1.0mmol aniline, after stirring for 5 minutes, 1.0mmol cyclohexanone was added, placed in a water bath reactor with magnetic stirring, and the reaction was carried out at room temperature at 25°C for 3 hours. TLC followed the reaction until the reaction was complete. The reaction result is: 2-(phenyl(anilino)methyl)cyclohexanone, the yield is 100%, and the selectivity of 2-(phenyl(anilino)methyl)cyclohexanone is 100%.
preparation example 3
[0040] Add 0.05mmol organic bismuth ion compound (R 1 , R 2 , R 3 , R 4 =C 2 h 5 , R 5 , R 6 , R 7 , R 8 = H, X = OSO 2 CF 3 ) and 2.0mL ethanol, 1.0mmol benzaldehyde and 1.0mmol aniline, after stirring for 5 minutes, 1.0mmol cyclohexanone was added, placed in a water bath reactor with magnetic stirring, and the reaction was carried out at room temperature at 25°C for 3 hours. TLC followed the reaction until the reaction was complete. The reaction result is: 2-(phenyl(anilino)methyl)cyclohexanone, the yield is 100%, and the selectivity of 2-(phenyl(anilino)methyl)cyclohexanone is 100%.
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