Table 3 Synthesis of 2‐amino‐4H‐chromene derivatives using creatine-based catalyst.
Entry | Aldehyde | Product | Time (min) | Yielda (%) | Mp (°C) | ||
|---|---|---|---|---|---|---|---|
Observed | Literature | ||||||
1 | 4-nitrobenzaldehyde | 4a | 5 | 96 | 176–182 | 176–18356 | |
2 | 3-nitrobenzaldehyde | 4b | 4 | 96 | 204–207 | 204–20657 | |
3 | 2-chlorobenzaldehyde | 4c | 4 | 96 | 212–215 | ||
4 | 3-chlorobenzaldehyde | 4d | 7 | 92 | 228–232 | 229–23260 | |
5 | 4-chlorobenzaldehyde | 4e | 6 | 94 | 214–217 | 214–21659 | |
6 | 3-methylbenzaldehyde | 4f | 10 | 88 | 197–200 | 198–20061 | |
7 | 4-methylbenzaldehyde | 4g | 10 | 86 | 215–219 | 215–21862 | |
8 | 4-isopropylbenzaldehyde | 4h | 12 | 91 | 196–200 | 198–20061 | |
9 | 2-methoxybenzaldehyde | 4i | 12 | 84 | 202–204 | 203–20756 | |
10 | 3-methoxybenzaldehyde | 4j | 8 | 86 | 197–200 | 197–19963 | |
11 | 4-methoxybenzaldehyde | 4k | 10 | 86 | 194–197 | ||
12 | 3,4,5-trimethoxybenzaldehyde | 4l | 9 | 91 | 175–177 | 175–17967 | |
13 | 3-hydroxybenzaldehyde | 4m | 15 | 82 | 233–235 | 232–23468 | |
14 | 4-hydroxybenzaldehyde | 4n | 18 | 81 | 208–210 | 208–21069 | |
15 | 2,4-dichlorobenzaldehyde | 4o | 6 | 94 | 118–120 | 118–12070 | |
