Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2272-29-9 | HCID 16763 | — |
| Catalyst | 18-Crown-6 | HCID 28557 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 791000 | HCID 791000 | 46% |
Reaction Steps
To a mixture of (4-chloro-phenyl)-(4,6-dichloro-[1,3,5]triazin-2-yl)amine (3.97 g, 14.4 mmol), potassium carbonate (2.20 g, 15.9 mmol) and 18-crown-6 (46 mg, 0.17 mmol) in toluene (25 ml), cooled in an ice bath, was added a solution of aniline (1.4 ml, 15.4 mmol) in toluene (10 ml) over 15 minutes. After stirring at room temperature for 24 hours, the mixture was treated with ethyl acetate (35 ml) and filtered through a pad of celite under suction. The filtrate was concentrated under vacuum and the residue was recrystallized (chloroform) to give 6-Chloro-N-(4-chlorophenyl)-N′-phenyl[1,3,5]triazine-2,4-diamine (2.20 g, 46% yield) as a white solid. 1H NMR (d6-DMSO) δ 10.1–10.4 (2 H, br s), 7.5–7.8 (4 H, br s), 7.3–7.5 (4 H, m), 7.15–7.05 (1 H, m), ESMS m/z 330 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07064125B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-80a5f85608ce423395023b0dcc1fb4ce |
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| Source note | uspto-grants-2006_06 |
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