Synthetic method of 2-hydroxypyridine compound
A technology of hydroxypyridine and synthesis method, applied in directions such as organic chemistry, can solve the problems of high raw material price, low yield, many synthesis steps, etc., and achieves the effects of fewer steps, simple synthesis process, and improved yield
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Embodiment 1
[0032] Put 2,6-dichloropyridine (4kg, 26.8mol) and tert-butanol (16L) into a 50L kettle, prepare a solution of sodium tert-butoxide (4kg, 41.7mol) in tert-butanol (6.5L), and add it to the kettle , warmed to reflux, reacted for 16 hours, removed tert-butanol, added 10.7 L of water to the solid, and adjusted the pH value to 5-6 with concentrated hydrochloric acid, added 40% (v / v) HBr aqueous solution, heated and stirred overnight, cooled and filtered, 2.5 kg of beige crystals of 6-chloro-2-hydroxypyridine were obtained, with a yield of 70%.
Embodiment 2
[0034] 2,3-Dichloropyridine (1740g, 11.76mol) and tert-butanol (9L) were added to a 20L kettle, sodium tert-butoxide (2032g, 21.17mol) was added to the reaction solution, the temperature was raised to reflux, and the reaction solution gradually Thin and easy to stir, reflux for 16 hours to remove tert-butanol, add 4.7L of water to the solid and adjust the pH value to neutral with concentrated HCl, add 40% HBr (800ml) and heat and stir for 6 hours, then cool to precipitate 3-chloro-2-hydroxypyridine Off-white crystal 1050g, yield 70%.
Embodiment 3
[0036] Add 2-chloro-3-picoline (1275g, 10mol) and tert-butanol (8L) into a 20L kettle, add sodium tert-butoxide (2032g, 21.17mol) into the reaction solution, raise the temperature to reflux, and react for 16h , to remove tert-butanol, add 4L of water to the solid and adjust the pH value to 5-6 with concentrated HCl, add 40% HBr (1000ml) and heat and stir for 10h, cool and precipitate 708g of off-white crystals of 3-methyl-2-hydroxypyridine, and collect rate of 65%.
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