Use of bismuth nitrate and iron nitrate as nitrification agent in aromatic compound nitrification
The technology of an aromatic compound and a nitrating reagent is applied in the application field of bismuth nitrate and ferric nitrate as nitrating reagents in the nitration reaction of aromatic compounds, which can solve the difficulty in recovering the acetic anhydride nitrating reagent, cannot be simply recycled, and uses a phase transfer catalyst. and other problems, to achieve the effect of low price, easy storage and easy access
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Embodiment 1
[0036] Weigh phenol 107mg, Bi(NO 3 ) 3 ·5H 2 Add 485mg of O and 1ml of acetone into a 10ml ground-mouthed round bottom flask, stir the reaction at 25°C, the reaction is exothermic and completes quickly, filter with a sand core funnel, and use CH 2 Cl 2 Wash the solids, combine the filtrates, concentrate to about 1ml, and separate with thin layer chromatography. The developer is selected from the mixed solvent of cyclohexane: ether=1:1 to obtain 72 mg of o-nitrophenol and 74 mg of p-nitrophenol. The yields are respectively 46% and 47%, and the total yield is 93%.
Embodiment 2
[0038] Weigh p-cresol 108mg, Bi(NO 3 ) 3 ·5H 2 Add 245mg of O and 2ml of dichloromethane into a 10ml ground-mouth round bottom flask, stir and react in a water bath at 10°C, and filter with a sand core funnel for 12 hours, and use CH 2 Cl 2 Wash the solids, combine the filtrates, evaporate most of the solvent, concentrate to about 1ml, separate by thin-layer chromatography, and develop with a mixed solvent of cyclohexane and ether to obtain 110mg of 2-nitro-4methylphenol with a yield of 72%. .
Embodiment 3
[0040] Weigh o-cresol 108mg, Fe(NO 3 ) 3 9H 2 Add 135mg of O and 0.5ml of diethyl ether into a 10ml ground-mouth round bottom flask, stir and react at 0°C for 15 hours, filter through a sand core funnel, and use CH 2 Cl 2 Wash the solids, combine the filtrates, evaporate most of the solvent, concentrate to about 1ml, separate by thin layer chromatography, and develop with a mixed solvent of cyclohexane and ether to obtain 65 mg of 2-methyl-6 nitrophenol, 2-methyl -4-Nitrophenol 78 mg, yields were 42% and 51%, total yield 93%.
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