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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30398생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/30398

반응식

참여 물질

역할이름HCID투입량
반응물CyclooctylamineHCID 2903—
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물Trimesoyl chlorideHCID 78138—
반응물Lithium ChlorideHCID 433294—
용매PyridineHCID 1049—
생성물1,3,5-Benzenetricarboxylic acid tris(cyclooctylamide)HCID 59789613—

반응 조건

온도5 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423088B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-0249888884cf4a97b3e2384f1b38319c
출처 메모uspto-grants-2008_09