返回
化工社化工社化学信息打印报告 · 仅供科研参考
HRID 61321生成日期:2026年10月26日

甲基丙烯酰氯 → 1,2,3-苯三甲酸

https://huagongshe.com/reaction/61321

反应方程式

参与物

角色名称HCID投料
反应物甲基丙烯酰氯HCID 13528—
反应物氢氧化钠HCID 14798—
反应物氯酸溶液HCID 19654—
反应物1-氨基苯-3,4,5-三羧酸HCID 14434861—
溶剂聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
产物1,2,3-苯三甲酸HCID 11288—

反应条件

温度10 °C

反应步骤

A 2 litter flask equipped with a magnetic stirrer, a thermometer, and 250 ml dripping funnel were filled with 1 litter of water and 71 g of sodium hydroxide pellet. When this was dissolved, 100 g of 1-aminobenzene-3,4,5-tricarboxylic acid was added and dissolved. After neutralization heat ceased, the reaction result was cooled down to 10° C. The dripping funnel was filled with 40.23 g of methacryloyl chloride. While this was maintained below 15° C., the liquid was dripped to the reaction container in 15 minutes. 40 g of sodium hydroxide was dissolved in 150 g of water in another container. This solution was added to the reaction mixture 20 minutes after the addition of methacryloyl chloride was complete. After the reaction product was cooled down to 10° C., 40 g of methacryloyl chloride was dripped from the dripping funnel in 15 minutes while the temperature was maintained below 15° C. 20 minutes after the dripping was complete, the reaction mixture was acidized to pH 3 by strong chloric acid. The thus-produced solid portion was extracted by vacuum filtration followed by washing with ethanol and dried at 60° C. for 14 hours in a vacuum oven.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US09441129B2
来源数据集uspto-grants-2016_09
ORD IDord-da715e30b7b54c4082e65d2c95077131
来源说明uspto-grants-2016_09