Table 1.
Optimized Suzuki‐Miyaura coupling reaction conditions.
|
| ||||||
|---|---|---|---|---|---|---|
| Entry | Base | Solvent | Pd (mol%) | Time (min) | Temp (°C) | Yield (%)a |
| 1 | K2CO3 | EtOH/H2O(1:1) | 0 | 180 | 80 | 0 |
| 2 | K2CO3 | EtOH/H2O(1:1) | 0.3 | 30 | 80 | 98 |
| 3 | K2CO3 | EtOH/H2O(1:1) | 0.3 | 15 | 80 | 98 |
| 4 | K2CO3 | EtOH/H2O(1:1) | 0.3 | 90 | 40 | 65 |
| 5 | K2CO3 | EtOH/H2O(1:1) | 0.3 | 90 | r.t | 50 |
| 6 | K2CO3 | EtOH/H2O(1:1) | 0.3 | 15 | 60 | 98 |
| 7 | K2CO3 | H2O | 0.3 | 30 | 60 | 50 |
| 8 | K2CO3 | EtOH | 0.3 | 30 | 60 | 50 |
| 9 | K2CO3 | MeCN | 0.3 | 30 | 60 | 60 |
| 10 | K2CO3 | THF | 0.3 | 30 | 60 | 45 |
| 11 | K2CO3 | DMSO | 0.3 | 30 | 60 | 68 |
| 12 | K2CO3 | DMF | 0.3 | 30 | 60 | 70 |
| 13 | K2CO3 | EtOH/H2O(1:1) | 0.2 | 15 | 60 | 77 |
| 14 | K2CO3 | EtOH/H2O(1:1) | 0.15 | 15 | 60 | 56 |
| 15 | No base | EtOH/H2O(1:1) | 0.3 | 30 | 60 | 4 |
Reaction condition: phenylboronic acid (0.6 mmol), base (0.4 mmol), Iodobenzene (0.5 mmol), solvent (2 mL), nanocatalyst (0.3 mol%).
aIsolated yield.