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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501814Generated: November 1, 2026

Hydrochloric Acid → HCID 13170167, compound

https://huagongshe.com/reaction/501814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactant4-BromobenzaldehydeHCID 70741—
ReactantPotassium AcetateHCID 517044—
CatalystTriphenylphosphineHCID 11776—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcrylateHCID 8821—
ProductHCID 13170167HCID 13170167—

Reaction Conditions

Temperature90 °C

Reaction Steps

5.00 g of 4-bromobenzaldehyde was dissolved in 100 mL of N,N-dimethylformamide, to which 2.9 mL of ethyl acrylate, 0.30 g of palladium(II) acetate, 0.35 g of triphenylphosphine, 13.20 g of potassium acetate, and 8.70 g of tetra-n-butylammonium bromide were added, and this solution was stirred for 2.5 hours at 90° C. The reaction mixture was added to a mixture of ethyl acetate and water, and adjusted to pH 2 with 6M hydrochloric acid, and the organic phase was separated therefrom. After the resultant organic phase was washed with water and a saturated sodium chloride solution successively, the washed phase was dried over anhydrous magnesium sulfate, and the solvent was distilled out under reduced pressure. The resultant residue was purified by silica gel column chromatography [eluent; hexane:ethyl acetate=2:1] to yield 4.75 g of ethyl (E)-3-(4-formylphenyl)-2-propenoate as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772285B2
Source datasetuspto-grants-2010_08
ORD IDord-4e85852a1c8b49a0ae98822f4bc10298
Source noteuspto-grants-2010_08