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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063781Generated: November 2, 2026

Ethanol → 2,2-Dimethyl-6-(4-methylphenyl)-2,3-dihydro-1-benzofuran

https://huagongshe.com/reaction/2063781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant6-Bromo-2,2-dimethyl-2,3-dihydrobenzofuranHCID 11138857—
Reactant4-Methylphenyl dihydrogen borateHCID 19035350—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
Product2,2-Dimethyl-6-(4-methylphenyl)-2,3-dihydro-1-benzofuranHCID 6676078556%

Reaction Conditions

Temperature150 °C

Reaction Steps

4-methylphenylboric acid (1.35 g, 9.91 mmol), tetrakis(triphenylphosphine)palladium (382 mg, 0.331 mmol), an aqueous solution of 2N sodium carbonate (4.5 mL) and ethanol (83 mL) were sequentially added to a solution of dimethoxyethane (9 mL) containing 6-bromo-2,2-dimethyl-2,3-dihydro-1-benzofuran (1.50 g, 6.61 mmol) synthesized in Reference Example 7, and the mixture was stirred under microwave irradiation at 150° C. for 10 minutes. After cooled to room temperature, water was added to the reaction solution, and extraction was performed using ethyl acetate. The extract was washed with saturated sodium hydrogencarbonate and saturated saline, and then dried using anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate 99:1 to 93/7) to give 880 mg of the title compound (yield: 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288390B2
Source datasetuspto-grants-2012_10
ORD IDord-8ef069e61ed444269fa3b4cdf7bb1a52
Source noteuspto-grants-2012_10