Method for preparing salicylaldehyde by oxidizing saligenol selectively catalyzed by molecular oxygen
A technology of salicyl alcohol and molecular oxygen, which is applied to the preparation of carbon-based compounds, chemical instruments and methods, and the preparation of organic compounds. It can solve the problems of many by-products, high cost, and low yield, and achieve low cost and pollution. Small size and high reaction efficiency
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Embodiment 1
[0027] The feed ratio is as follows: salicyl alcohol: 2,2,6,6-tetramethylpiperidine-N-oxyl radical (TEMPO): sodium bromide-sodium bromate combination: sodium nitrite: sulfuric acid with a molar ratio of 1 :0.01:0.048:0.08:0.075, wherein the molar ratio of sodium bromide-sodium bromate combination is 5:1:
[0028] Add 0.62g (5mmol) salicyl alcohol, 0.0078g (0.05mmol) TEMPO, 0.021g (0.2mmol) NaBr, 0.0063g (0.04mmol) NaBrO to a 50ml Erlenmeyer flask 3 , 5ml 1,2-dichloroethane, 0.5ml water, add 0.018ml concentrated sulfuric acid dropwise, stir for 5 minutes, then add 0.0276g (0.4mmol) NaNO2, react at 25°C for 7 hours in an air atmosphere, and analyze by gas chromatography Product composition. After the reaction, the reaction solution was washed with saturated Na 2 S 2 o 3 The solution is washed, acidified, extracted, dried, and then distilled at atmospheric pressure to remove the solvent, and then distilled with a vacuum distillation device to collect fractions at about 84-86 ...
Embodiment 2
[0030] The feed ratio is as follows: salicyl alcohol: 2,2,6,6-tetramethylpiperidine-N-oxyl radical (TEMPO): sodium bromide-sodium bromate combination: sodium nitrite: hydrochloric acid with a molar ratio of 1 :0.01:0.04:0.08:0.06, wherein the molar ratio of sodium bromide-sodium bromate combination is 5:1:
[0031]Add 0.62g (5mmol) salicyl alcohol, 0.0078g (0.05mmol) TEMPO, 0.016g (0.16mmol) NaBr, 0.0063g (0.04mmol) NaBrO to a 50ml Erlenmeyer flask 3 , 5ml dichloromethane, 1ml water, dropwise added 0.014ml hydrochloric acid, stirred for 15 minutes, then added 0.0276g (0.4mmol) NaNO 2 , reacted at 10°C for 12 hours under an oxygen atmosphere, and analyzed the composition of the product by gas chromatography. After the reaction, the reaction solution was washed with saturated Na 2 S 2 o 3 The solution is washed, acidified, extracted, dried, and then distilled at atmospheric pressure to remove the solvent, and then distilled with a vacuum distillation device to collect fracti...
Embodiment 3
[0033] The feed ratio is as follows: salicyl alcohol: 2,2,6,6-tetramethylpiperidine-N-oxyl radical (TEMPO): sodium bromide-sodium bromate combination: sodium nitrite: sulfuric acid with a molar ratio of 1 :0.01:0.01:0.1:0.015, wherein the molar ratio of sodium bromide-sodium bromate combination is 3:1:
[0034] Add 0.62g (5mmol) salicyl alcohol, 0.0078g (0.05mmol) TEMPO, 0.0039g (0.0375mmol) NaBr, 0.0019g (0.0125mmol) NaBrO to a 50ml Erlenmeyer flask 3 , 5ml acetonitrile, 0.5ml water, dropwise add 0.004ml concentrated sulfuric acid, stir for 10 minutes, then add 0.035g (0.5mmol) NaNO 2 , reacted at 80°C for 15 hours under an air atmosphere, and analyzed the composition of the product by gas chromatography. After the reaction, the reaction solution was washed with saturated Na 2 S 2 o 3 The solution is washed, acidified, extracted, dried, and then distilled at atmospheric pressure to remove the solvent, and then distilled with a vacuum distillation device to collect fractio...
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