HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839593Generated: October 25, 2026
Sodium Carbonate → 4-(2,6-difluoro-phenyl)-1H-indole
https://huagongshe.com/reaction/1839593
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-Bromo-2,6-difluorobenzene | HCID 123557 | — |
| Reactant | 1H-Indole-4-boronic acid, pinacol ester | HCID 11322471 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(2,6-difluoro-phenyl)-1H-indole | HCID 22561702 | 91.5% |
Reaction Steps
To a mixture of 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indole (11.34 g, 46.6 mmol), and 1-bromo-2,6-difluorobenzene (9 g, 46.6 mmol) in 1,2-dimethoxyethane (204 mL) were added Palladium catalyst Pd(PPh3)4 (1.62 g, 1.4 mmol) and the freshly prepared sodium carbonate solution (15.19 g in 66 mL of 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 110° C. oil bath for overnight. 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 with brine, and dried over Na2SO4. After filtration, the solvents were evaporated, and the crude product was purified by a silica gel column to give 9.77 g (91%) of 4-(2,6-difluoro-phenyl)-1H-indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06677368B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-9b7545f77ae94d63ab76b8c89d6696c1 |
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| Source note | uspto-grants-2004_01 |
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