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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423217Generated: October 30, 2026

Sodium Carbonate → 3-(2-tert-butylphenyl)-1-(phenylsulfonyl)-1H-indole

https://huagongshe.com/reaction/2423217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1,4-DioxaneHCID 31275—
Reactant1-(phenylsulfonyl)-1H-indol-3-ylboronic acidHCID 2776217—
Reactant2-(Tert-butyl)phenyl trifluoromethanesulfonateHCID 18779207—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product3-(2-tert-butylphenyl)-1-(phenylsulfonyl)-1H-indoleHCID 6724193792%

Reaction Conditions

Temperature150 °C

Reaction Steps

1-(Phenylsulfonyl)-1H-indol-3-ylboronic acid (150.9 mg, 0.501 mmol), 2-tert-butylphenyl trifluoromethanesulfonate (255 mg, 0.902 mmol) and tetrakis(triphenylphosphine)palladium (0) (58 mg, 0.050 mmol) are combined in a septa capped microwave vial and placed under an argon atmosphere. Degassed solutions of 2 M sodium carbonate (0.75 mL, 1.50 mmol) and of dioxane (2.5 mL) were introduced and the vial heated to 150° C. for 15 minutes in a microwave reactor. The cooled reaction mixture was diluted with water and ethyl acetate, the phases separated and the aqueous extracted twice more with ethyl acetate. The combined extracts were washed with water, brine, dried over sodium sulfate, filtered and evaporated. The residue was purified by silica gel chromatography eluting with a gradient of ethyl acetate and hexanes to give 3-(2-tert-butylphenyl)-1-(phenylsulfonyl)-1H-indole (175.8 mg, 92%) as a colorless gummy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960569B2
Source datasetuspto-grants-2011_06
ORD IDord-2feede511ec445e48403e3681e1b83cf
Source noteuspto-grants-2011_06