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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 专利号 | US09441129B2 |
|---|
| 来源数据集 | uspto-grants-2016_09 |
|---|
| ORD ID | ord-da715e30b7b54c4082e65d2c95077131 |
|---|
| 来源说明 | uspto-grants-2016_09 |
|---|