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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523505Generated: October 31, 2026

Potassium Carbonate → 3-Benzyl-3-methyl-2,3-dihydro-benzofuran-6-carboxylic acid methyl ester

https://huagongshe.com/reaction/523505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
Reactant4-Iodo-3-(2-methyl-allyloxy)-benzoic acid methyl esterHCID 25129045—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product3-Benzyl-3-methyl-2,3-dihydro-benzofuran-6-carboxylic acid methyl esterHCID 2512904695.1%

Reaction Conditions

Temperature115 °C

Reaction Steps

To a solution of 4-Iodo-3-(2-methyl-allyloxy)-benzoic acid methyl ester (455 mg, 1.37 mmol) obtained in Example 4(A), in DMF (15 mL) were added Potassium carbonate (379 mg, 2.74 mmol), Tetrabutylammonium chloride (380 mg, 1.37 mmol), Palladium acetate (25.6 mg, 0.136 mmol) in DMF (5 mL) and Phenylboronic acid (200 mg, 1.64 mmol). The resulting mixture was stirred for 3 h at 115° C., cooled to room temperature, filtered over silica, washed with water, dried over MgSO4 and concentrated. Column chromatography (silica gel, heptane/CH2Cl2: 4/6) afforded 368 mg (95%) of the title compound as a slightly brown oil which crystallize. Mp: 52° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09339486B2
Source datasetuspto-grants-2016_05
ORD IDord-a4a9d3b1439d40fea69b58a3deac4e60
Source noteuspto-grants-2016_05