Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Fluorophenylboronic acid | HCID 285645 | — |
| Reactant | 6-Bromoindole | HCID 676493 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-(4-FLUOROPHENYL)INDOLE | HCID 11106658 | 65.2% |
Reaction Steps
Step 1 A mixture of 6-bromo-1H-indole (0.25 g, 1.275 mmol), 4-fluorophenylboronic acid (0.178 g, 1.275 mmol), and 2 M aqueous sodium carbonate (2.0 mL, 4.00 mmol) in toluene (10 mL) and ethanol (2.500 mL) was purged with argon and treated with tetrakis(triphenylphosphine)palladium (0.074 g, 0.064 mmol). The mixture was heated at 90° C. After 17 h, the mixture was cooled to rt and partitioned between water and EtOAc. The organic phase was dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from 95:5 to 60:40 hexane-EtOAc) to provide 6-(4-fluorophenyl)-1H-indole as a white solid (175.5 mg, 65%). 1H NMR (400 MHz, DMSO-d6) δ 11.17 (1 H, br. s.), 7.65-7.71 (2 H, m), 7.56-7.62 (2 H, m), 7.37 (1 H, t, J=2.9 Hz), 7.22-7.31 (3 H, m), 6.44 (1 H, t, J=2.0 Hz). Mass spectrum m/z 212.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362065B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-f7b6effe5b9f4c3090b8ce544423651a |
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| Source note | uspto-grants-2013_01 |
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