Synthetic method of 2-chloro-5-chloromethyl pyridine
A technology of chloromethylpyridine and synthesis method, which is applied in the field of organic chemical synthesis, can solve the problem of high by-products of 2-chloro-5-trichloromethylpyridine, and achieve the effect of reducing the generation of by-products
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Embodiment 1
[0018] Add 10g of 3-picoline, 30mL of nitrobenzene and 45ml of buffer solution into a four-neck flask, adjust the pH value of the solution to about 4 with dilute hydrochloric acid, and add 0.2g of phosphorus trichloride at the same time. Introduce nitrogen, electromagnetically stir, heat up to 80°C, stop nitrogen flow and switch to chlorine gas, continue to heat up to 120°C, under constant temperature, chlorine gas bubbling reaction for 12h, stop heating, close the chlorine gas injection valve, pass in nitrogen gas, bubbling Soak chlorine for 1h. After the reaction solution was distilled off under reduced pressure, a brown-red oily liquid was obtained. The product was purified by high vacuum fractional distillation, and the distillate was collected. After extraction with chloroform, the extracts were combined, and after desolvation under reduced pressure, 18.9 g of a light yellow oily liquid was obtained, and the yield of the product 2-chloro-5-trichloromethylpyridine was 89....
Embodiment 2
[0020] Add 10g of 3-picoline, 25mL of nitrobenzene and 25ml of buffer solution into a four-neck flask, adjust the pH value of the solution to about 4.5 with dilute hydrochloric acid, and add 0.3g of phosphorus trichloride at the same time. Introduce nitrogen, electromagnetically stir, heat up to 100°C, stop nitrogen flow and switch to chlorine gas, continue to heat up to 140°C, under constant temperature, chlorine gas bubbling reaction for 16h, stop heating, close the chlorine gas sampling valve, pass in nitrogen gas, bubbling Soak chlorine for 1h. After the reaction solution was distilled off under reduced pressure, a brown-red oily liquid was obtained. The product was purified by high vacuum fractional distillation, and the distillate was collected. After extraction with chloroform, the extracts were combined, and after desolvation under reduced pressure, 19.4 g of a light yellow oily liquid was obtained, and the yield of the product 2-chloro-5-trichloromethylpyridine was 9...
Embodiment 3
[0021] Add 10g of 3-picoline, 45mL of nitrobenzene and 90ml of buffer solution into a four-neck flask, adjust the pH value of the solution to about 5 with dilute hydrochloric acid, and add 0.5g of phosphorus trichloride at the same time. Introduce nitrogen, electromagnetically stir, heat up to 90°C, stop nitrogen flow and switch to chlorine gas, continue to heat up to 160°C, under constant temperature, chlorine gas bubbling reaction for 20h, stop heating, close the chlorine gas injection valve, pass in nitrogen gas, bubbling Soak chlorine for 1h. After the reaction solution was distilled off under reduced pressure, a brown-red oily liquid was obtained. The product was purified by high vacuum fractional distillation, and the distillate was collected. After extraction with chloroform, the extracts were combined, and after desolvation under reduced pressure, 19.1 g of a light yellow oily liquid was obtained, and the yield of the product 2-chloro-5-trichloromethylpyridine was 90....
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