HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982977Generated: October 30, 2026
1-Bromo-3-fluorobenzene → HCID 12079630, compound
https://huagongshe.com/reaction/982977
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-3-fluorobenzene | HCID 14082 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1H-Indole-4-boronic acid, pinacol ester | HCID 11322471 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 12079630 | HCID 12079630 | 89% |
Reaction Steps
To a mixture of 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl) 1H-indole (3, 2.43 g, 10 mmol), and 3-bromofluorobenzene (1.09 mL, 10 mmol) in THF (34 mL)) were added Palladium catalyst Pd(PPh3)4 (347 mg, 0.3 mmol) and the freshly prepared sodium hydroxide solution (1.20 g, 30 mmol in 14 mL water). The system was degassed and then charged with nitrogen. The degas procedure was repeated for three times. The mixture was stirred under nitrogen at 70° C. oil bath for 15 hours. TLC showed the completion of the coupling reaction. The mixture was cooled to room temperature, diluted with ethyl acetate, and separated from water layer. The ethyl acetate solution was washed by brine, dried over Na2SO4, and concentrated. The crude product was purified by a silica gel column eluting with hexanes-EtOAc (9:1) to provide 1.88 g (88%) of the product 4-(3-fluoro-phenyl)-1H-indole as a colorless syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06861418B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-fdbbfc22752b413a9671d5e37c554848 |
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| Source note | uspto-grants-2005_03 |
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