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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217423Generated: October 29, 2026

Sodium Carbonate → Methyl 5-isopropenyl-4-phenylthiophene-2-carboxylate

https://huagongshe.com/reaction/217423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
ReactantAmmonium ChlorideHCID 25517—
Reactant4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolaneHCID 10997426—
ReactantMethyl 5-bromo-4-phenylthiophene-2-carboxylateHCID 58438859—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 5-isopropenyl-4-phenylthiophene-2-carboxylateHCID 58438695—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of methyl 5-bromo-4-phenylthiophene-2-carboxylate in dioxane were added 2-isopropenyl-4,4,5,5-tetramethyl 1,3,2-dioxaborolane and a 2 M aqueous Na2CO3 solution. To the reaction mixture were added palladium acetate and PPh3, followed by stirring at 100° C. for 5 hours. After leaving to be cooled, a saturated aqueous NH4Cl solution was added thereto, followed by extraction with EtOAc. The organic layer was washed with brine, dried over MgSO4, and then concentrated under reduced pressure, followed by purification by silica gel column chromatography (hexane:EtOAc=95:5 to 80:20) to obtain methyl 5-isopropenyl-4-phenylthiophene-2-carboxylate as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193378B2
Source datasetuspto-grants-2012_06
ORD IDord-91d753e1e34f4132959a8a5fe9a9dfc8
Source noteuspto-grants-2012_06