反应详情

温度

70 °C

In a 3 L-reaction flask, 156.8 g (0.45 mol) of 3-oxo-2-(2-phenyl-5-ethyl-1,2,3-triazol-4-yl)-3-(1,3,4-trimethylpyrazol-5-yl)propionitrile and 900 g of xylene were added, the temperature was raised to 70° C., and 162.7 g (1.35 mol) of pivaloyl chloride was added dropwise under reflux over 10 hours while removing hydrogen chloride under a reduced pressure at 68 to 71° C./10 to 13 kPa. After reacting as such for 5 hours, 740 g of a mixture of pivaloyl chloride and xylene was distilled off at 70° C. under a reduced pressure in order to remove excess pivaloyl chloride. After adding 156 g of warm water of 70° C., 70 g of 2.7% sodium hydrogen carbonate aqueous solution was added dropwise. After separating the resulting aqueous phase, the resulting organic phase was washed with 156 g of warm water of 70° C., the resulting aqueous phase was separated to obtain a xylene solution containing 181 g (yield 93.0%) of (2E)-3-(2,2-dimethylpropanoyloxy)-2-(2-phenyl-5-ethyl-1,2,3-triazol-4-yl)-3-(1,3,4-trimethylpyrazol-5-yl)acrylonitrile. After distilling off most of xylene at 90° C. under a reduced pressure, 540 g of acetonitrile was added, and crystallization was carried out by gradually cooling from 70° C. After stirring at 0° C. for 1 hour, the resulting crystal was filtered, and dried to obtain 163.5 g (yield 84%) of (2E)-3-(2,2-dimethylpropanoyloxy)-2-(2-phenyl-5-ethyl-1,2,3-triazol-4-yl)-3-(1,3,4-trimethylpyrazol-5-yl)acrylonitrile (melting point: 119° C.).

1. additionwere added
2. temperatureunder reflux over 10 hours
3. customwhile removing hydrogen chloride under a reduced pressure at 68 to 71° C./10 to 13 kPa
4. customsuch for 5 hours
5. distillation740 g of a mixture of pivaloyl chloride and xylene was distilled off at 70° C. under a reduced pressure in order
6. customto remove excess pivaloyl chloride
7. additionAfter adding 156 g of warm water of 70° C., 70 g of 2.7% sodium hydrogen carbonate aqueous solution
8. additionwas added dropwise
9. customAfter separating the resulting aqueous phase
10. washthe resulting organic phase was washed with 156 g of warm water of 70° C.
11. customthe resulting aqueous phase was separated
12. customto obtain a xylene solution