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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923728Generated: October 28, 2026

Potassium Carbonate → 4-(3,5-Di-t-butylphenyl)indene

https://huagongshe.com/reaction/923728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant4-Bromo-1H-indeneHCID 15637624—
Reactant2-(3,5-Di-tert-butylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 58471046—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventWaterHCID 962—
Product4-(3,5-Di-t-butylphenyl)indeneHCID 2202303963%

Reaction Conditions

Temperature80 °C

Reaction Steps

Mixture of compound 4 (60 g, 308 mmol, 1 equiv), 2-(3,5-di-tert-butylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (126 g, 400 mmol, 1.3 equiv), powdered potassium carbonate (128 g, 924 mmol, 3 equiv) and bis(triphenylphosphine)palladium(II)dichloride (25.3 g, 31 mmol, 0.1 equiv), 1,4-dioxane (300 mL) and water (150 mL) was heated overnight at 80° C. The reaction was poured into 700 mL of water and extracted with ethyl acetate (3×500 mL). The combined organic layers were washed with saturated brine (1 L), dried over sodium sulfate, and concentrated under reduced pressure. The resulting residue was purified over silica gel (1 Kg) eluting with heptanes to give compound 5 (59 g, 63% yield) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09279024B2
Source datasetuspto-grants-2016_03
ORD IDord-48c018fd171840d9811245b1615b1682
Source noteuspto-grants-2016_03