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HRID 30398作成日:2026年10月25日

Cyclooctylamine → 1,3,5-Benzenetricarboxylic acid tris(cyclooctylamide)

https://huagongshe.com/reaction/30398

反応式

関与物質

役割名称HCID仕込み量
反応物CyclooctylamineHCID 2903—
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物Trimesoyl chlorideHCID 78138—
反応物Lithium ChlorideHCID 433294—
溶媒PyridineHCID 1049—
生成物1,3,5-Benzenetricarboxylic acid tris(cyclooctylamide)HCID 59789613—

反応条件

温度5 °C

反応手順

4.20 g (33 mmol) of cyclooctylamine and 0.1 g of dry LiCl are added under inert atmosphere to 70 ml of dry NMP and 15 ml of dry pyridine and cooled to 5° C. Then, 2.39 g (9 mmol) of 1,3,5-benzenetricarboxylic acid trichloride are added. The reaction mixture is heated to 75° C. and stirred. After 2 hours the reaction mixture is added to 300 ml of ice water. Customary work-up (recrystallization from N,N-dimethylformamide) gives 1,3,5-benzenetricarboxylic acid tris(cyclooctylamide).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423088B2
出典データセットuspto-grants-2008_09
ORD IDord-0249888884cf4a97b3e2384f1b38319c
出典メモuspto-grants-2008_09