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Suzuki: the reaction was carried out in a 25 mL vessel, at 130°C in a time range of 3-24 h. In a typical run, a mixture of aryl halide (10 mmol, boronic acid (15 mmol, aq K3PO4 (20 mmol, and catalyst (10-20 mol, in 3 mL of o-xylene was stirred for the desired time. The solution was allowed to cool, and a 1:1 mixture of Et2O-H 2O (20 mL) was added. The organic layer was washed, separated, further washed with another 10 mL portion of Et2O, dried with anhyd MgSO4, and filtered. The solvent and volatiles were completely removed under vacuum to give the crude product which subjected to column chromatographic separation resulted in pure compounds. The reaction was followed by GC-MS. At the end of the process, the mixture of reaction was filtered; the residue of support-containing catalyst washed to completely remove the remains of products and/or reactants and used again
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4, and filtered. The solvent and volatiles were completely removed under vacuum to give the crude product which subjected to column chromatographic separation resulted in pure compounds. The reaction was followed by GC-MS. At the end of the process, the mixture of reaction was filtered; the residue of support-containing catalyst washed to completely remove the remains of products and/or reactants and used again.
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4 (20 mmol) and catalyst (10-20 mol%) in 3 mL of o-xylene was stirred for the desired time. The reaction was followed by GC-MS. At the end of the process, the mixture of reaction was filtered; the residue of support-containing catalyst washed to completely remove the remains of products and/or reactants, and used again.
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4 (20 mmol) and catalyst (10-20 mol%) in 3 mL of o-xylene was stirred for the desired time. The reaction was followed by GC-MS. At the end of the process, the mixture of reaction was filtered; the residue of support-containing catalyst washed to completely remove the remains of products and/or reactants, and used again.
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