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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982995Generated: October 25, 2026

Sodium Carbonate → 4-(2,6-difluoro-phenyl)-1H-indole

https://huagongshe.com/reaction/982995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-Bromo-2,6-difluorobenzeneHCID 123557—
Reactant1H-Indole-4-boronic acid, pinacol esterHCID 11322471—
CatalystPalladiumHCID 23938—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
Product4-(2,6-difluoro-phenyl)-1H-indoleHCID 2256170291.5%

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06861418B2
Source datasetuspto-grants-2005_03
ORD IDord-aeff157433714a52bad26c59625b8a2f
Source noteuspto-grants-2005_03