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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283682Generated: October 26, 2026

Potassium Phosphate, Tribasic → Methyl 5-methoxy-3-methylbenzo[b]thiophene-2-carboxylate

https://huagongshe.com/reaction/2283682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantMethylboronic AcidHCID 139377—
ReactantMethyl 3-chloro-5-methoxy-1-benzothiophene-2-carboxylateHCID 2801561—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 5-methoxy-3-methylbenzo[b]thiophene-2-carboxylateHCID 12561472—

Reaction Conditions

Temperature100 °C

Reaction Steps

Methyl boronic acid (120 mg), potassium phosphate (849 mg), water (0.30 ml), palladium acetate (22 mg), and 2-dicyclohexylphosphino-2′,4′,6′-triisopropyl biphenyl (95 mg) were added to a solution of methyl 3-chloro-5-methoxy-1-benzothiophene-2-carboxylate (257 mg) in 1,4-dioxane (3.0 ml), and the reaction solution was stirred at 100° C. for 12 hours. The reaction solution was diluted with ethyl acetate and washed successively with an aqueous ammonium chloride solution, an aqueous sodium bicarbonate solution, and a saturated saline solution. After drying over anhydrous sodium sulfate, the solvent was evaporated under vacuum. The resultant residue was purified by column chromatography on silica gel (developing solvent:hexane-ethyl acetate) to obtain methyl 5-methoxy-3-methylbenzo[b]thiophene-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145414B2
Source datasetuspto-grants-2015_09
ORD IDord-ade2f2939fc04385b686a0b1e7d7f253
Source noteuspto-grants-2015_09