Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10902369 | HCID 10902369 | 57% |
Reaction Steps
To a mixture of 18.5 g (0.1 mol) of cyanuric chloride and 50 mL of acetonitrile was added a mixed solution of 9.9 g (0.1 mol) of cyclohexlamine, 10.1 g (0.1 mol) of triethylamine and 35 mL of water over 2 hours by keeping the reaction temperature not to exceed 5° C. Thereafter, the stirring was continued for 2 hours while maintaining the temperature at 5° C. or lower. Subsequently, 70 mL of an aqueous 28% ammonia solution was dropwise added at the same temperature, followed by stirring at 5° C. for 1 hour, at 20° C. for 1 hour, and at 50° C. for 2 hours. Thereafter, 54.5 g (0.55 mol) of cyclohexylamine was dropwise added at a reaction temperature of 60° C. and the mixture was stirred at 70° C. for 3 hours. To the reaction mixture thus obtained was added 180 g of water, and the mixture was cooled down to 10° C. while continuing the stirring to precipitate crystals, which were collected by filtration, washed 5 times with 80 mL of water, and dried under reduced pressure to obtain 16.5 g (yield 57%) of the titled compound. Melting point: 153° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06127538 |
|---|
| Source dataset | uspto-grants-2000_10 |
|---|
| ORD ID | ord-e554941d53554de48fa33de3fca6b89a |
|---|
| Source note | uspto-grants-2000_10 |
|---|