Table 3.
Synthesis of 4H-chromene derivatives using g-C3N4@l-arginine nanocatalyst.
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|---|---|---|---|---|---|---|
| Entry | R | Product | Time (min) | Mp (°C) | Mp (°C, ref.) | Yield (%) |
| 1 | H | 9a | 7 | 228–229 | 225–228 33 | 95 |
| 2 | 4-Cl | 9b | 10 | 210–212 | 211–213 33 | 97 |
| 3 | 4-NO2 | 9c | 15 | 178–179 | 177–179 34 | 88 |
| 4 | 2,4-Cl | 9d | 10 | 118–120 | 115–117 24 | 95 |
| 5 | 4-OH | 9e | 20 | 206–208 | 208–210 24 | 93 |
| 6 | 4-Me | 9f. | 30 | 217–220 | 220–221 35 | 91 |
| 7 | 3-NO2 | 9g | 20 | 206–207 | 206–209 34 | 93 |
| 8 | 2-Cl | 9h | 15 | 213–214 | 211–213 35 | 96 |
| 9 | 4-CN | 9i | 25 | 184–187 | 184–186 35 | 89 |
| 10 | 4-OMe | 9j | 30 | 203–204 | 196–19833 | 87 |
Reaction conditions: Reaction of benzaldehyde (1 mmol), dimedone (1 mmol), and malononitrile (1 mmol) g-C3N4@l-arginine (20 mg) and ethanol (7 mL) under reflux conditions.
