Research Article
A Green and Efficient Method for the Preparation of 3,4-Dihydropyrimidin-2(1H)-ones Using Quaternary Ammonium-Treated Clay in Water
Table 1
Optimization of experimental conditions for synthesis of DHPMs.
| Entry | Catalyst | Temperature | Time (h) | Result |
| 1 | CTAB-modified clay (0.02 g)
| Reflux | 0.5 | Not completed, 44% yield | 2 | CTAB-modified clay (0.04 g)
| Reflux | 0.5 | Not completed, 77% yield | 3 | CTAB-modified clay (0.05 g)
| Reflux | 0.5 | Completed, 89% yield | 4 | CTAB-modified clay (0.05 g)
| r.t | 0.5 | Not completed, 35% yield | 5 | Clay | Reflux | 0.5 | No reaction |
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Reaction conditions: benzaldehyde (1 mmol), acetylacetone (1 mmol), and urea (1.5 mmol).
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