1,2-disubstituted ally/arylox yphthalate compounds and use thereof
A technology of aryloxybenzoic acid and di-substitution, applied in the field of aryloxybenzoic acid 1
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[0039] Example: Synthesis of 5-(2-chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoic acid 2-(methoxycarbonyl)-1-phenylallyl ester (compound 1) :
[0040]
[0041] Add III-1 (11.6 grams, 0.032 moles, available from the market) and 150 milliliters of methylene chloride in a 250-ml reaction flask, stir, add oxalyl chloride (6.1 grams, 0.048 moles), 2 drops of DMF, stir at room temperature for 5 hours, concentrated to obtain 11.0 g of acid chloride, the appearance of which was yellow liquid (IV-1).
[0042]
[0043] Add V-1 (0.58 grams, 3.0 mmoles) in the reaction bottle of 50 milliliters, triethylamine (0.46 grams), 5 milliliters of dichloromethanes, drip IV-1 (1.2 grams, 3.2 millimoles) under stirring cooling The mixed solution of 10 ml of dichloromethane was added in about half an hour, and the reaction was carried out at room temperature for 6 hours. After the reaction was completed, 100 ml of dichloromethane and 50 ml of water were added to the reaction liquid, and the...
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