HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanuric chloride → HCID 20153015, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Piperazinone, 1-[2-(cyclohexylamino)ethyl]-3,3,5,5-tetramethyl- | HCID 15165099 | — |
| Reactant | 2,4,6-Tris[cyclohexyl[2-(3,3,5,5-tetramethyl-2-oxo-1-piperazinyl)ethyl]amino]-1,3,5-triazine | HCID 22622815 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20153015 | HCID 20153015 | — |
Reaction Steps
In a manner analogous to that described hereinabove, a compound identified as 2,4,6-tris[cyclohexyl[2-(3,3,5,5-tetramethyl-2-oxo-1-piperazinyl)ethyl]amino]-1,3,5-triazine which has the following structure: ##STR27## is prepared by reacting 0.046 mole 1-[2-(cyclohexylamino)ethyl]-3,3,5,5-tetramethyl-2-piperazinone and 0.01 mole cyanuric chloride, 1.2 g sodium hyroxide and 150 ml toluene. The reaction was carried out at 200° C. for 10 hr. The resulting light straw colored solid isolated was recrystallized from acetone and analyzed. It had a m p of 179°-180° C. and was off-white in color.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04480092 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-a3bd93c4726f4ccdad0c38fc12032f5b |
| Source note | uspto-grants-1984_10 |