Method for preparing scutellarin
A technology of scutellarin and dichloroethane, which is applied in the preparation of sugar derivatives, chemical instruments and methods, sugar derivatives, etc., can solve the problems of difficult industrial application, cumbersome process operation, high price, etc., and achieve high-efficiency chemical synthesis. The effect of preparation, operation safety, easy production control
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Embodiment 1
[0041] Example 1: The preparation method of this scutellarin is as follows:
[0042] (1) Synthesis of Compound 3: Weigh 23.5g (0.25mol) of phenol into a 1000ml round bottom flask, add 300ml of methanol and 130ml of commercially available hydrobromic acid with a concentration of 47% by mass, and then slowly Add 90ml of hydrogen peroxide with a mass percent concentration of 30% dropwise therein, and control the dropping rate so that the temperature of the reaction solution does not exceed 40°C, and the addition is completed in about 1 to 2 hours. After addition, continue to stir for 1-2 hours, add a little sodium bisulfite, filter after a few minutes, wash the filter cake with a small amount of methanol, press dry, and dry at 70-80°C to obtain a white powdery solid, namely compound 3; Weighing: 82.0g, yield: 98%. 1 HNMR (DMSO): δ9.92(s, 1H), δ7.46(s, 2H).
[0043] (2) Synthesis of Compound 4: Weigh 84.0g (1.5mol) of sodium methoxide into a 1000ml round bottom flask, add 200m...
Embodiment 2
[0058] Example 2: The preparation method of this scutellarin is as follows:
[0059] (1) Synthesis of Compound 3: Weigh 23.5g (0.25mol) of phenol into a 1000ml round bottom flask, add 500ml of ethanol, 80g (0.78mol) of sodium bromide and 20ml (0.40mol) of commercially available 98% concentrated sulfuric acid , then slowly add 90ml of hydrogen peroxide with a mass percentage concentration of 30% to it under vigorous stirring at room temperature, control the rate of addition so that the temperature of the reaction solution does not exceed 45°C, and add it in about 1-2 hours; after the addition, continue to stir for 1- After 2 hours, add a little sodium bisulfite, filter after a few minutes, wash the filter cake with a small amount of distilled water, press dry, and dry at 70-80°C to obtain a white powdery solid, that is, compound 3. Weighing: 82.0g, yield: 99%. 1 HNMR (DMSO): same as step (1) of Example 1 above.
[0060] (2) Synthesis of compound 4: Weigh 84.0g (1.5mol) of s...
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