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. 2023 Feb 3;13:2001. doi: 10.1038/s41598-023-27800-3

Table 1.

Optimized Suzuki‐Miyaura coupling reaction conditions.

graphic file with name 41598_2023_27800_Figa_HTML.gif
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.