A kind of synthetic method of 2,3-dichloropyridine
A technology of dichloropyridine and a synthesis method, applied in directions such as organic chemistry, can solve the problems of high price, no industrial production value, large amount of catalyst, etc., and achieves the effect of high industrial value
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Embodiment 1
[0019] In a 250ml autoclave, put 30g2,3,6-trichloropyridine, 90g ethanol, 30g triethylamine, 0.5g tris(triphenylphosphine)rhodium chloride (I), 1g triphenylphosphine into Nitrogen replaces the air in the reaction kettle. After the replacement, hydrogen is passed through and the temperature is raised to 80°C for reaction. During the reaction, the reaction pressure gradually decreases, and hydrogen is added to maintain the reaction pressure between 0.8 and 1.0 MPa. The reaction is continued for 20 hours, and the reaction ends. Sampling and analysis showed that the conversion rate of 2,3,6-trichloropyridine was 97%, the selectivity of 2,3-dichloropyridine was 89%, and the yield of 2,3-dichloropyridine was 86.3%.
Embodiment 2
[0021] In a 250ml autoclave, drop into 30g2,3,6-trichloropyridine, 90g ethanol, 30g triethylamine, 0.08g tris(triphenylphosphine) rhodium chloride (I), 0.2g triphenylphosphine, pass Inject nitrogen to replace the air in the reactor. After the replacement, pass hydrogen and raise the temperature to 83°C for reaction. During the reaction, the reaction pressure gradually decreases. Add hydrogen to maintain the reaction pressure between 0.8 and 1.0 MPa. Continue the reaction for 26 hours, and the reaction ends. Sampling and analysis showed that the conversion rate of 2,3,6-trichloropyridine was 93%, the selectivity of 2,3-dichloropyridine was 89%, and the yield of 2,3-dichloropyridine was 82.8%.
Embodiment 3
[0023] In a 250ml autoclave, drop into 30g2,3,6-trichloropyridine, 90g ethanol, 30g triethylamine, 0.08g tris(triphenylphosphine) rhodium chloride (I), 0.3g triphenylphosphine, pass Inject nitrogen to replace the air in the reaction kettle. After the replacement, pass hydrogen and raise the temperature to 83°C for reaction. During the reaction, the reaction pressure gradually decreases. Add hydrogen to maintain the reaction pressure between 0.8 and 1.0 MPa. Continue the reaction for 24 hours, and the reaction ends. The conversion rate of 2,3,6-trichloropyridine was 95%, the selectivity of 2,3-dichloropyridine was 90%, and the yield of 2,3-dichloropyridine was 85.5%.
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