Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735870Generated: October 25, 2026

Triethylamine → Ethyl 3-{3,5-difluoro-2-[2-(ethoxycarbonyl)vinyl]phenyl}acrylate

https://huagongshe.com/reaction/1735870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcrylateHCID 8821—
Reactant1,2-Dibromo-3,5-difluorobenzeneHCID 2724517—
CatalystHydrazine hydrate (1:1)HCID 24654—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-{3,5-difluoro-2-[2-(ethoxycarbonyl)vinyl]phenyl}acrylateHCID 53722136126.7%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 1,2-dibromo-3,5-difluorobenzene (24.7 g, 91.6 mmol) , bis (triphenylphosphine)palladium(II) chloride (2.57 g, 3.66 mmol) and triethylamine (51.0 mL, 366 mmol) in 300 mL of DMF was stirred under argon at approximately 85° C. for 15 minutes. Hydrazine hydrate (366 μL, 7.54 mmol) was added and the mixture was stirred for an additional 10 minutes. Ethyl acrylate (39.7 mL, 366 mmol) was added and the mixture was stirred under argon at approximately 85° C. for approximately 144 hours. The solvents were removed by evaporation under reduced pressure and the residue was dissolved in 1.0 L of ethyl acetate. The ethyl acetate solution was washed 3 times with water and dried over magnesium sulfate. Evaporation of the solvent gave crude ethyl 3-{3,5-difluoro-2-[2-(ethoxycarbonyl)vinyl]phenyl}acrylate (36 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05538988
Source datasetuspto-grants-1996_07
ORD IDord-c33fda0cd4b848408f99df712fe12728
Source noteuspto-grants-1996_07