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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177241Generated: October 30, 2026

Ethyl Acrylate → HCID 131732999, compound

https://huagongshe.com/reaction/2177241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromo-2,6-difluorophenolHCID 2736292—
CatalystPalladium ChlorideHCID 24290—
SolventDimethylformamideHCID 6228—
ProductHCID 131732999HCID 131732999—

Reaction Conditions

Temperature80 °C

Reaction Steps

Into a 250-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 4-bromo-2,6-difluorophenol (6.3 g, 30.15 mmol, 1.00 equiv), ethyl prop-2-enoate (17.2 g, 171.80 mmol, 5.70 equiv), P(toly)3 (18.24 g), DIEA (11.6 g, 89.76 mmol, 2.98 equiv), PdCl2 (0.531 g), N,N-dimethylformamide (100 mL). The resulting solution was stirred overnight at 80° C. The reaction was then quenched by the addition of 30 mL water. The resulting solution was extracted with 3×50 mL of ethyl acetate and the organic layers combined and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (30/70). The collected fractions were combined and concentrated under vacuum. This resulted in 6 g (79%) of ethyl (2Z)-3-(3,5-difluoro-4-hydroxyphenyl)prop-2-enoate as yellow oil. Mass spectrum (ESI, m/z): Calcd. for C11H10F2O3, 229.1 (M+H). found 229.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067898B1
Source datasetuspto-grants-2015_06
ORD IDord-1101ab8841c3497186bdae44d54ca5a0
Source noteuspto-grants-2015_06