Catalyst for catalyzing synthesis of indoxacarb key intermediate and application of catalyst
A technology for catalyzing indanes and catalysts, which is applied in the directions of organic compound/hydride/coordination complex catalysts, physical/chemical process catalysts, organic chemistry, etc., and can solve the problems of large amount of catalyst, high production cost, low catalyst efficiency, etc. , to achieve the effect of enhancing selectivity, reducing dosage, and facilitating industrialization
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Embodiment 1
[0039] Prepare a chiral catalyst and use the catalyst to prepare indoxacarb. The specific preparation method is as follows:
[0040] (1) Add 3.26g (0.01mol) of quinidine hydrochloride to a 1000mL clean and anhydrous reaction flask, then add 50mL of toluene, heat up to 60°C and stir to dissolve.
[0041] (2) Weigh 1.25 g (0.01 mol) of manganese chloride, and add it to the toluene solution of the above-mentioned hydroquinidine.
[0042] (3) Heating up to 80° C., reacting for 2 hours to obtain a clear and transparent chiral catalyst solution.
[0043] The method for preparing S-body indoxacarb using the above-mentioned catalyst can adopt the conventional synthesis route disclosed in the master’s degree thesis "Synthetic Technology and Polymorphic Form of Novel and High-efficiency Chiral Insecticide Indoxacarb" awarded by Zhejiang University in 2014. in:
[0044] (4) Add 225g tert-butyl hydroperoxide and 449g 5-chloro-2-methoxycarbonyl-1-indanone ester and 500mL toluene to the c...
Embodiment 2
[0047] Prepare a chiral catalyst and use the catalyst to prepare indoxacarb. The specific preparation method is as follows:
[0048] (1) Add 4.89g (0.015mol) of quinidine hydrochloride to a 1000mL clean and anhydrous reaction flask, then add 50mL of toluene, heat up to 60°C and stir to dissolve.
[0049] (2) Weigh 1.51 g (0.01 mol) of manganese sulfate, and add it into the above-mentioned toluene solution of quinidine hydrochloride.
[0050] (3) Heating up to 80° C., reacting for 2 hours to obtain a clear and transparent chiral catalyst solution.
[0051] The method for preparing S-body indoxacarb using the above-mentioned catalyst can adopt the conventional synthesis route disclosed in the master’s degree thesis "Synthetic Technology and Polymorphic Form of Novel and High-efficiency Chiral Insecticide Indoxacarb" awarded by Zhejiang University in 2014. in:
[0052] (4) add 113g tert-butyl hydroperoxide and 224g 5-chloro-2-methoxycarbonyl-1-indanone ester and 600mL toluene t...
Embodiment 3
[0055] Prepare a chiral catalyst and use the catalyst to prepare indoxacarb. The specific preparation method is as follows:
[0056] (1) Add 6.52g (0.02mol) of quinidine hydrochloride to a 1000mL clean and anhydrous reaction flask, then add 50mL of toluene, heat up to 60°C and stir to dissolve.
[0057] (2) Weigh 0.89g (0.01mol) of manganese hydroxide, and add it into the above-mentioned toluene solution of quinidine hydrochloride.
[0058] (3) Heating up to 80° C., reacting for 2 hours to obtain a clear and transparent chiral catalyst solution.
[0059] The method for preparing S-body indoxacarb using the above-mentioned catalyst can adopt the conventional synthesis route disclosed in the master’s degree thesis "Synthetic Technology and Polymorphic Form of Novel and High-efficiency Chiral Insecticide Indoxacarb" awarded by Zhejiang University in 2014. in:
[0060] (4) add 169g tert-butyl hydroperoxide and 336g 5-chloro-2-methoxycarbonyl-1-indanone ester and 600mL toluene to...
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