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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228255Generated: October 30, 2026

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

https://huagongshe.com/reaction/2228255

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 numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-392bcda1c5cf4269bd1865cb0eb0c170
Source noteuspto-grants-2002_07