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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclooctylamine | HCID 2903 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Trimesoyl chloride | HCID 78138 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1,3,5-Benzenetricarboxylic acid tris(cyclooctylamide) | HCID 59789613 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423088B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-0249888884cf4a97b3e2384f1b38319c |
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| Source note | uspto-grants-2008_09 |
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