Preparation method of 2,3-dimethoxybenzoyl chloride
A technology of dimethoxybenzoyl and dimethoxyformyl, applied in the field of medicine, can solve the problems of low yield, complex synthesis process, unstable yield and the like
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Embodiment 1
[0007] Embodiment 1: the preparation of 2,3-dimethoxybenzoyl chloride:
[0008] Add 1821 mg of 2,3-dimethoxybenzoic acid to the reactor, add 40 ml of tetrahydrofuran, stir, add 0.5 ml of N,N-dimethylformamide at room temperature, then stir at room temperature for 0.5 hours, drop 3 g of thionyl chloride, and then continued to stir the reaction at room temperature for 8 hours. After the reaction was completed, the compound 2,3-dimethoxybenzoyl chloride was obtained through the post-treatment and purification process with a yield of 81.8%.
Embodiment 2
[0009] Embodiment 2: the preparation of 2,3-dimethoxybenzoyl chloride:
[0010] Add 1821 mg of 2,3-dimethoxybenzoic acid to the reactor, add 40 ml of tetrahydrofuran, stir, add 0.5 ml of N,N-dimethylformamide at room temperature, then stir at room temperature for 0.5 hours, drop 3 g of thionyl chloride, and then continued to stir the reaction at room temperature for 8 hours. After the completion of the reaction, the compound 2,3-dimethoxybenzoyl chloride was obtained through post-treatment and purification process with a yield of 82.9%.
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