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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839571Generated: October 26, 2026

Potassium Acetate → Indole

https://huagongshe.com/reaction/1839571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
Reactant4-BromoindoleHCID 676494—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantDiborateHCID 86587655—
CatalystPalladiumHCID 23938—
SolventDimethyl SulfoxideHCID 679—
ProductIndoleHCID 79821.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 4-bromoindole (1, 9.80 g, 50 mmol), pinacole diborate (2, 13.97 g, 55 mmol), and KOAc (14.72 g, 150 mmol) in DMSO (200 mL) was added Palladium catalyst PdCl2(dppf) CH2Cl2 (1.22 g, 1.5 mmol). The system was degassed, and then charged with nitrogen for three times. The mixture was stirred at 80° C. oil bath under nitrogen for 22 hours. TLC2 showed the complete disappearance of the starting material 4-bromoindole (1). The mixture was cooled to room temperature, and then poured to water (1 L). The product was extracted with ethyl acetate for three times. The combined extracts were washed by brine for five times to remove DMSO solvent, and then dried over Na2SO4. During the washing step, the catalyst may precipitate out, which was removed by filtration. The ethyl acetate solution was filtered and condensed. The residue was purified on a silica gel column eluting with EtOAc-hexane (9:1). The first fraction provided the side product indole (1.25 g, 21% yield), Rf 0.55 (EtOAc-Hexane 5:1). The second fraction provided the product 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indole as a white solid (3, 8.01 g, 66%), Rf 0.46 (EtOAc-Hexane 5:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677368B2
Source datasetuspto-grants-2004_01
ORD IDord-40d715fbdb1d41c0a84251f67bace9c9
Source noteuspto-grants-2004_01