Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Diisopropylaminoethanol | HCID 7313 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 87176092 | HCID 87176092 | — |
Reaction Steps
To 27.6 g (190 mmole) of 2-(diisopropylamino)ethanol, 6.83 g (81 mmole) of sodium bicarbonate, and 1.3 mL (70 mmole) of deionized water at room temperature was added 5.0 g (27 mmole) of cyanuric chloride. The temperature of the solution was raised to 30° C. and stirred for 1 hour at which time the evolution of carbon dioxide ceased. The temperature of the solution was raised to 45° C. and stirring was continued overnight. After cooling, the mixture was filtered, and the solids rinsed with methylene chloride. The combined filtrates were concentrated in vacuo to 6 g of 2-chloro-4,6-di-(2-(diisopropylamino)ethoxy)-1,3,5-triazine as a liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07867774B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-58e74cf30b094bda837fad850afab2bf |
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| Source note | uspto-grants-2011_01 |
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