HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxide → 4,6-Dichloro-N-(1,1,3,3-tetramethylbutyl)-1,3,5-triazin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxide | HCID 961 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | tert-Octylamine | HCID 61017 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4,6-Dichloro-N-(1,1,3,3-tetramethylbutyl)-1,3,5-triazin-2-amine | HCID 6430809 | — |
Reaction Conditions
| Temperature | 9 °C |
|---|
Reaction Steps
Into a flask, 20 grams of water, 52.3 grams (0.284 mole) of cyanuric chloride and 130 grams of mixed xylenes having a boiling point of 138-141° C. were charged, and 37.5 grams (0.290 mole) of 1,1,3,3-tetramethylbutylamine was slowly and dropwise added into the mixture while maintaining the temperature at 8-10° C. Then, 57.9 grams of 20% aqueous hydroxide solution was slowly and dropwise added into the mixture while keeping the temperature at 8-10° C. After the reaction was complete, the oil (organic) and water phases were separated and the water phase was removed to obtain a xylene solution of 2,4-dichloro-6-(1,1,3,3-tetramethylbutylamino)-1,3,5-triazine,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06469165B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-73a2093f6ca849a89c22813aa0bf9c4e |
| Source note | uspto-grants-2002_10 |