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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277242Generated: November 3, 2026

Ethyl Acetate → methyl (E)-3-[5-(4-tert-butylphenyl)thiophen-2-yl]acrylate

https://huagongshe.com/reaction/1277242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant(E)-methyl 3-(5-bromothiophen-2-yl)acrylateHCID 25417100—
Reactant4-Tert-butylphenyl borateHCID 86756165—
SolventEthanol toluene waterHCID 86587398—
Productmethyl (E)-3-[5-(4-tert-butylphenyl)thiophen-2-yl]acrylateHCID 8675617785.8%

Reaction Steps

Under argon atmosphere, a solution of methyl (E)-3-(5-bromothiophen-2-yl)acrylate (0.23 g), 4-tert-butylphenyl borate (0.3 g) and potassium carbonate (0.26 g) in toluene/ethanol/water (20/2/2 ml) was stirred at room temperature for 1 hour. To the mixture was added tetrakistriphenylphosphine palladium (32 mg), and the mixture was refluxed for 18 hours and then cooled to room temperature. To the organic layer was added ethyl acetate, and the mixture was washed with saturated brine and dried with magnesium sulfate. Under reduced pressure, the mixture was concentrated, and the residue was purified with column chromatography (ethyl acetate/hexane=1:9) to give pale yellow crystals of methyl (E)-3-[5-(4-tert-butylphenyl)thiophen-2-yl]acrylate (240 mg). This compound was used for the following reaction, without subjecting further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166006
Source datasetuspto-grants-2000_12
ORD IDord-9a5505ea241441868d2b213529781e4f
Source noteuspto-grants-2000_12