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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64430Generated: October 29, 2026

Potassium Carbonate → tert-butyl (2E)-3-(3-formyl-2-thienyl)acrylate

https://huagongshe.com/reaction/64430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl acrylateHCID 15458—
Reactant2-Bromothiophene-3-carbaldehydeHCID 12245921—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Producttert-butyl (2E)-3-(3-formyl-2-thienyl)acrylateHCID 86713442—

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 1 g of 2-bromothiophene-3-carbaldehyde, 3.8 ml of tert-butyl acrylate, 120 mg of palladium acetate, 420 mg of tetra-n-butylammonium bromide, and 610 mg of potassium carbonate in 10 ml of DMF was stirred at 100° C. overnight. After leaving to be cooled, the insoluble material was filtered through Celite, and to the filtrate were added water and ethyl acetate to carry out a layer separation operation. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 660 mg of tert-butyl (2E)-3-(3-formyl-2-thienyl)acrylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447090B2
Source datasetuspto-grants-2016_09
ORD IDord-ed9ee36aef7240c194eee930d48cb9d9
Source noteuspto-grants-2016_09