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. 2023 Jun 7;13(25):17143–17154. doi: 10.1039/d2ra08347g

Preparation of various organic compounds by Suzuki coupling reaction under optimum conditionsa.

graphic file with name d2ra08347g-u2.jpg
Entry Aryl boronic acid Aryl halide Product Time (min) Yield (%)
1 graphic file with name d2ra08347g-u3.jpg graphic file with name d2ra08347g-u4.jpg graphic file with name d2ra08347g-u5.jpg 60 92
2 graphic file with name d2ra08347g-u6.jpg graphic file with name d2ra08347g-u7.jpg graphic file with name d2ra08347g-u8.jpg 60 95
3 graphic file with name d2ra08347g-u9.jpg graphic file with name d2ra08347g-u10.jpg graphic file with name d2ra08347g-u11.jpg 60 97
4 graphic file with name d2ra08347g-u12.jpg graphic file with name d2ra08347g-u13.jpg graphic file with name d2ra08347g-u14.jpg 60 99
5 graphic file with name d2ra08347g-u15.jpg graphic file with name d2ra08347g-u16.jpg graphic file with name d2ra08347g-u17.jpg 60 77
6 graphic file with name d2ra08347g-u18.jpg graphic file with name d2ra08347g-u19.jpg graphic file with name d2ra08347g-u20.jpg 92 92
7 graphic file with name d2ra08347g-u21.jpg graphic file with name d2ra08347g-u22.jpg graphic file with name d2ra08347g-u23.jpg 60 95
8 graphic file with name d2ra08347g-u24.jpg graphic file with name d2ra08347g-u25.jpg graphic file with name d2ra08347g-u26.jpg 60 99
9 graphic file with name d2ra08347g-u27.jpg graphic file with name d2ra08347g-u28.jpg graphic file with name d2ra08347g-u29.jpg 60 98
10 graphic file with name d2ra08347g-u30.jpg graphic file with name d2ra08347g-u31.jpg graphic file with name d2ra08347g-u32.jpg 60 99
11 graphic file with name d2ra08347g-u33.jpg graphic file with name d2ra08347g-u34.jpg graphic file with name d2ra08347g-u35.jpg 60 98
12 graphic file with name d2ra08347g-u36.jpg graphic file with name d2ra08347g-u37.jpg graphic file with name d2ra08347g-u38.jpg 73 99
13 graphic file with name d2ra08347g-u39.jpg graphic file with name d2ra08347g-u40.jpg graphic file with name d2ra08347g-u41.jpg 60 76
14 graphic file with name d2ra08347g-u42.jpg graphic file with name d2ra08347g-u43.jpg graphic file with name d2ra08347g-u44.jpg 60 95
15 graphic file with name d2ra08347g-u45.jpg graphic file with name d2ra08347g-u46.jpg graphic file with name d2ra08347g-u47.jpg 60 90
16 graphic file with name d2ra08347g-u48.jpg graphic file with name d2ra08347g-u49.jpg graphic file with name d2ra08347g-u50.jpg 60 98
17 graphic file with name d2ra08347g-u51.jpg graphic file with name d2ra08347g-u52.jpg graphic file with name d2ra08347g-u53.jpg 60 96
18 graphic file with name d2ra08347g-u54.jpg graphic file with name d2ra08347g-u55.jpg graphic file with name d2ra08347g-u56.jpg 90 99
19 graphic file with name d2ra08347g-u57.jpg graphic file with name d2ra08347g-u58.jpg graphic file with name d2ra08347g-u59.jpg 60 97
20 graphic file with name d2ra08347g-u60.jpg graphic file with name d2ra08347g-u61.jpg graphic file with name d2ra08347g-u62.jpg 60 95
21 graphic file with name d2ra08347g-u63.jpg graphic file with name d2ra08347g-u64.jpg graphic file with name d2ra08347g-u65.jpg 93 35
a

Conditions for the chemical reaction: 1 mmol of aryl halide, 1 mmol of aryl boronic acid, 70 °C, EtOH 78%, K2CO3.