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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410263Generated: October 31, 2026

Methyl Acrylate → (E)-methyl 3-(2-fluoropyridin-3-yl)acrylate

https://huagongshe.com/reaction/410263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantN-Methyl dicyclohexylamineHCID 24210—
Reactant3-Bromo-2-fluoropyridineHCID 2762778—
ReactantBis(cyclohexylmethyl)amineHCID 4594378—
CatalystHCID 178418851HCID 178418851—
Solvent1,4-DioxaneHCID 31275—
Product(E)-methyl 3-(2-fluoropyridin-3-yl)acrylateHCID 5932706795%

Reaction Conditions

Temperature110 °C

Reaction Steps

To Pd[P(t-Bu)3]2 (0.210 g, 0.411 mmol) was added dioxane (6 mL), methyl acrylate (2.00 mL, 22.2 mmol), N,N-dicyclohexylmethylamine (3.60 mL, 17.0 mmol), and 3-bromo-2-fluoropyridine (1.02 g, 5.80 mmol). The reaction mixture was degassed and heated to 110° C. for 5 min. The reaction was cooled to room temperature and diluted with EtOAc. The organic phase was washed with water (1×), brine (1×), dried over MgSO4, filtered, and concentrated. Purification by flash column chromatography on silica gel (10% to 50% EtOAc in hexanes) gave the product which contained Cy2NMe. The Cy2NMe was removed by dissolving the mixture in DCM (5 mL) and diluting with hexanes (10 mL). The solution was concentrated to a volume of 5 mL and the solid precipitate was collected by filtration and dried under high vacuum to give (E)-methyl 3-(2-fluoropyridin-3-yl)acrylate (0.995 g, 5.49 mmol, 95% yield) as a white solid. MS (ESI, pos. ion) m/z: 182.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759532B2
Source datasetuspto-grants-2014_06
ORD IDord-b31d5c7caa034d6e8b062e7557240b65
Source noteuspto-grants-2014_06