A kind of synthetic method of 4-amino-2-hydroxyl-3-isopropoxybenzoic acid
A technology of isopropoxybenzoic acid and synthesis method, applied in chemical instruments and methods, preparation of nitro compounds, preparation of carboxylate, etc., achieving high yield, simple operation and reasonable design
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[0036] A kind of synthetic method of 4-amino-2-hydroxyl-3-isopropoxybenzoic acid, this synthetic method comprises the steps:
[0037] (1) Under low temperature conditions, use dichloromethane as a solvent, pour raw materials A and triethylamine into the solvent and mix evenly, add acetyl chloride dropwise, after the dropwise addition, heat up, stir and react to obtain compound B; low temperature is -18~-3℃, the mass ratio of compound A, acetyl chloride and triethylamine is: 1.5~2.5:1:2~4, the solid-liquid g / mL ratio of compound A and dichloromethane is 1:12~14 ;
[0038] (2) Add compound B to dimethylformamide, lower the temperature, add sodium hydrogen, heat up, react, cool, add isopropyl bromide dropwise, after the dropwise addition, heat up and react to obtain compound C; compound B, sodium hydrogen, The mass ratio of isopropyl bromide is 6~7:2.5~3:4~5, and the solid-liquid g / mL ratio of compound B and dimethylformamide is 1:10~15; the preparation of compound C solution is...
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[0044] (1) Add 46g of compound A, 61g of triethylamine and 600mL of dichloromethane into the reaction flask, add 32g of acetyl chloride dropwise in an ice-water bath, after the drop is complete, heat up to 2,3°C and stir for 2h, detect by TLC, the reaction of the raw materials is complete , adding saturated sodium bicarbonate (300 ml), extracting with dichloromethane (500 ml*2), concentrating the organic phase, and column chromatography (mobile phase: n-hexane / ethyl acetate=50 / 1) to obtain 42.3 g of colorless Transparent oil, namely compound B, with a purity of 95.5% and a yield of 70.48%;
[0045] (2) Add 65g of compound B and dimethylformamide to the reaction bottle, cool to 0°C, add 30g of sodium hydrogen, react at 22°C for 2h, re-cool to 0°C, add 45g of isopropyl bromide dropwise, dropwise , heated to 25°C and reacted for 16 hours, TLC detection, the reaction of the raw materials was completed, the reaction solution was poured into 1000 ml of ice water, 6M hydrochloric aci...
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