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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30398Generated: October 25, 2026

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

https://huagongshe.com/reaction/30398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclooctylamineHCID 2903—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantTrimesoyl chlorideHCID 78138—
ReactantLithium ChlorideHCID 433294—
SolventPyridineHCID 1049—
Product1,3,5-Benzenetricarboxylic acid tris(cyclooctylamide)HCID 59789613—

Reaction Conditions

Temperature5 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423088B2
Source datasetuspto-grants-2008_09
ORD IDord-0249888884cf4a97b3e2384f1b38319c
Source noteuspto-grants-2008_09