Composition for preventing and removing pest
A technology for preventing and controlling harmful organisms, which is applied in biocides, organic chemistry, animal repellents, etc., and can solve problems such as difficult to control harmful organisms
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[0109] In the general formula shown in the following preparation method, X 1 、X 2 、X 3 、X 4 , Y 1 , Y 2 , Y 4 , Y 5 , G 1 , G 2 , R 1 , R 2 , Q 1 respectively can correspond to X 1 a.X 2 a.X 3 a.X 4 a.Y 1 a.Y 2 a.Y 4 a.Y 5 a.G 1 a.G 2 a. R 1 a. R 2 a.Q 1 a, it can also be the opposite. In addition, Q 2 It represents the meaning described in [1], or represents it as general formula (2), general formula (3), general formula (18).
[0110]
[0111] (where, Y 1 , Y 2 , Y 3 , Y 4 , Y 5 Indicates the same meaning as above. )
[0112]
[0113] (where, Y 6 , Y 7 , Y 8 , Y 9 Indicates the same meaning as above. )
[0114]
[0115] (where, Y 1 a.Y 2 a.Y 4 a.Y 5 a. R a , R b , R c Indicates the same meaning as above. )
[0116] Preparation method 1
[0117]
[0118] (where, A 1 、A 2 、A 3 、A 4 , G 1 , G 2 , R 1 , R 2 , X, n, Q 1 , Q 2 Represents the same meaning as above, and L represents a functional group having a lea...
Embodiment 1-1
[0635] Preparation of N-(2,6-Dimethyl-4-heptafluoroisopropyl)phenyl 3-nitrobenzamide
[0636] Add 20.0g of 2,6-dimethyl-4-heptafluoroisopropylaniline and 11.0g of pyridine into 100ml of tetrahydrofuran, stir at room temperature, and slowly drop into the resulting solution 13.0g of 3-Nitrobenzoyl chloride. After stirring at room temperature for 10 hours, ethyl acetate and water were added to the reaction solution. After liquid separation, the organic layer was separated and dried over anhydrous magnesium sulfate. This solution was filtered, the filtrate was collected, the solvent was distilled off under reduced pressure, and the obtained residue was washed with a mixed solvent of hexane-diisopropyl ether to obtain 26.0 g (yield 85%) of the target compound as a white solid.
[0637] 1 H-NMR (CDCl 3, ppm) δ2.33 (6H, s), 7.37 (2H, s), 7.68 (1H, s), 7.72 (1H, t, J=8.1Hz), 8.28 (1H, d, J=8.1Hz), 8.44(1H, dd, J=1.2, 8.1Hz), 8.75(1H, t, J=1.2Hz)
Embodiment 1-2
[0639] Preparation of N-(2,6-Dimethyl-4-heptafluoroisopropyl)phenyl 3-aminobenzamide
[0640] Add 0.90g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-nitrobenzamide and 1.56g of stannous chloride anhydrate into 25ml of ethanol, and stir at room temperature , 2 ml of concentrated hydrochloric acid was added to the resulting solution, and stirred at 60° C. for 1 hour. After returning to room temperature, the reaction solution was poured into water, and neutralization was performed using potassium carbonate. Ethyl acetate was added, and the insoluble matter was filtered off, and the organic layer was separated and dried over anhydrous magnesium sulfate. This solution was filtered, the filtrate was collected, the solvent was distilled off under reduced pressure, and the obtained residue was washed with hexane to obtain 0.44 g (yield 53%) of the target compound as a white solid.
[0641] 1 H-NMR (CDCl 3 , ppm) δ2.34 (6H, s), 3.87 (2H, broad), 6.86-6.89 (1H, m), 7.20-7.35 (...
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