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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (E)-methyl 3-(5-bromothiophen-2-yl)acrylate | HCID 25417100 | — |
| Reactant | 4-Tert-butylphenyl borate | HCID 86756165 | — |
| Solvent | Ethanol toluene water | HCID 86587398 | — |
| Product | methyl (E)-3-[5-(4-tert-butylphenyl)thiophen-2-yl]acrylate | HCID 86756177 | 85.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06413947B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-392bcda1c5cf4269bd1865cb0eb0c170 |
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| Source note | uspto-grants-2002_07 |
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