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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929615Generated: October 31, 2026

Butyl Acrylate → HCID 66733998, compound

https://huagongshe.com/reaction/1929615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl AcrylateHCID 8846—
ReactantDabcoHCID 9237—
ReactantPotassium CarbonateHCID 11430—
Reactant5-bromo-1,3-difluoro-2-methylbenzeneHCID 2783215—
Catalystpalladium(II) acetateHCID 167845—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 66733998HCID 66733998—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 5-bromo-1,3-difluoro-2-methyl-benzene (6.910 g; 33.379 mmol) in anhydrous DMF (200 ml) were added successively butyl acrylate (7.15 ml; 50.062 mmol), DABCO (157 mg; 1.333 mmol), potassium carbonate (4.612 g; 33.379 mmol), and palladium acetate (150 mg; 0.669 mmol). The resulting brown suspension was heated to 120° C. for 1 h. The reaction mixture was allowed to cool to rt before ether (400 ml) was added. This mixture was then washed with water (2×200 ml), and the mixed aq. layers were further extracted with ether (150 ml). The combined organic layers were dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure. Purification by FC (DCM/heptane=1/1=>DCM) gave the pure product 3-(3,5-difluoro-4-methyl-phenyl)-acrylic acid butyl ester as a yellow oil which was further dried under HV (4.690 g; 55%). LC-MS: tR=1.10 min.; [M+H]+: no ionisation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188082B2
Source datasetuspto-grants-2012_05
ORD IDord-482cf023f68c476b9ff7401d21f78deb
Source noteuspto-grants-2012_05