Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4,6-Dichloro-N,N-diethyl-1,3,5-triazin-2-aminato | HCID 74405 | — |
| Reactant | n-Butyl-2,2,6,6-tetramethyl-4-piperidinamine | HCID 118285 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 19768383 | HCID 19768383 | 66.4% |
Reaction Steps
4-n-Butylamino-2,2,6,6-tetramethylpiperidine (31.7 g, 149 mmol) is added over 15 minutes to a suspension of 15.0 g (67.8 mmol) of the 2,4-dichloro-6-diethylamino-1,3,5-triazine, 150 ml of xylene, and 7.0 g of powdered sodium hydroxide that had been heated to 70° C. The reaction mixture is heated at reflux for 23 hours. Sodium chloride is removed by filtration, and the filtrate is concentrated to a viscous oil. Further concentration of the oil by Kugelrohr distillation (140°-50° C., 0.05 mm) yields a residue which is crystallized from methanol-water to afford 25.8 g (66% yield) of 2,4-bis[N-(2,2,6,6-tetramethylpiperidin-4-yl)-n-butylamino]-6-diethylamino-1,3,5-triazine, m.p. 74°-76° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05204473 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-ad3d249c8f154474867d4890da36a4ec |
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| Source note | uspto-grants-1993_04 |
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