Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N~2~,N~4~-Dibutyl-6-chloro-1,3,5-triazine-2,4-diamine | HCID 14045984 | — |
| Product | Butylamine | HCID 8007 | — |
| Product | 2,4,6-tris(butylamino)-1,3,5-triazine | HCID 10891735 | — |
Reaction Steps
A solution of 150 millimoles of n-butylamine in 50 ml of dimethylacetamide was prepared and cooled to 0° C. To this solution was added at 0° C. a solution of 250 millimoles of diisopropylethylamine and 50 millimoles of N,N′-dibutyl-6-chloro-[1,3,5]triazine-2,4-diamine in 50 ml of dimethylacetamide, the resulting solution was heated under reflux for 4 hours, then cooled to room temperature, and the solvent was distilled off by an evaporator. The reaction mixture was then isolated and purified by silica gel column chromatography to give N,N′,N″-tributyl-[1,3,5]triazine-2,4,6-triamine as an oily substance. The result of 1H-NMR analysis is shown in FIG. 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198387B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-957b1d14799a401799e2b8bee0f9ed98 |
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| Source note | uspto-grants-2012_06 |
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