Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Dibutylamine | HCID 8148 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 135740159 | HCID 135740159 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 135740049 | HCID 135740049 | — |
Reaction Steps
21 ml of a 2.0 M solution of trimethylaluminium in hexane are added under argon to 5.5 g (0.042 mol) of dibutylamine in 35 ml of anhydrous dichloromethane. After 15 minutes, 10.5 g (0.014 mol) of 2,4,6-tris(4-[1-ethoxycarbonyl-1-methylethoxy]-2-hydroxyphenyl)-1,3,5-triazine (Compound 1) are added to the reaction mixture. After 1 day 10 ml of anhydrous xylene are added and the dichloromethane is distilled off. The reaction mixture is subsequently heated at 130° C. for 2 days and then 10 ml of 20% HCl are added. The reaction mixture is extracted with ethyl acetate and the organic phase is dried over magnesium sulfate. The title product is obtained after column chromatography (Compound 15: 1H NMR(CDCl3): 0.80 (t, J=7.1 Hz,9H), 0.90 (t, J=7.1 Hz,9H), 1.12-1.4 (m, 24H), 1.71 (s, 27H), 3.29-3.35 (m, 6H), 3.50-3.55 (m, 6H), 6.39-6.60 (m, 6H), 8.00-8.02 (m, 3H), 13.24 (s, 3H)) and also
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06346619B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-d48690578c844ed8a48f6edb60df1c00 |
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| Source note | uspto-grants-2002_02 |
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