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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191410Generated: November 4, 2026

Sodium Hydroxide → HCID 22561761, compound

https://huagongshe.com/reaction/2191410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-Bromo-2,3-difluorobenzeneHCID 2733260—
Reactant1H-Indole-4-boronic acid, pinacol esterHCID 11322471—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22561761HCID 2256176170%

Reaction Steps

4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indole 6b (1.22 g, 5 mmol) was dissolved in 20 ml of tetrahydrofuran under stirring, and added with 1-bromo-2,3-difluoro-benzene (0.97 g, 5 mmol), tetrakis (triphenylphosphine)palladium (0.17 g, 0.15 mmol) and sodium hydroxide solution (7 ml, 2 mol/L) under an argon atmosphere. Upon completion of the addition, the reaction system was stirred at 75° C. in an oil bath overnight. After thin lay chromatography showed the disappearance of starting materials, the reaction mixture was naturally cooled down to room temperature and extracted with ethyl acetate (20 ml×3). The combined organic extracts were washed with saturated brine (10 ml), dried over anhydrous sodium sulfate, filtered to remove the drying agent and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain 4-(2,3-difluoro-phenyl)-1H-indole 6c (800 mg, yield 70%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329682B2
Source datasetuspto-grants-2012_12
ORD IDord-d71cf85cd4054651a5144008aa07e511
Source noteuspto-grants-2012_12