Syntheses method of cinnamic acid/o-chlorobenzoic acid bagasse xylan diester with anti-HIV activity
A technology of o-chlorobenzoic acid and a synthesis method is applied in the synthesis field of anti-HIV active cinnamic acid/o-chlorobenzoic acid bagasse xylan diester, and can solve problems such as insufficient anti-HIV activity and the like
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[0036] (1) Put 20 g of bagasse xylan in a vacuum constant temperature drying oven at 50° C. and dry for 24 hours to obtain dry-based bagasse xylan.
[0037] (2) Weigh 15g of cinnamoyl chloride into a 50mL beaker, add 20mL of analytically pure dichloromethane, stir at room temperature for 7 minutes to obtain an esterifying agent solution, pour it into a 100mL constant pressure dropping funnel, and set aside.
[0038] (3) Weigh 15g of bagasse xylan obtained in step (1), place it in a 250mL four-necked flask equipped with a stirrer, a thermometer, and a reflux condensing device, then add 30mL of analytically pure dichloromethane, 3mL of analytically pure triethylamine, and stirred at room temperature for 30 minutes to obtain a bagasse xylan activation solution.
[0039] (4) Raise the temperature of the system in step (3) to 60° C., start to add the esterification agent solution prepared in step (2) dropwise, and control the dropping time to 4 hours. After the esterification agen...
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