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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55258Generated: October 25, 2026

Methyl Acrylate → (E)-Methyl 3-[3-(phenylmethoxy)pyridin-2-yl]-2-propenoate

https://huagongshe.com/reaction/55258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Benzyloxy-2-iodopyridineHCID 19957501—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product(E)-Methyl 3-[3-(phenylmethoxy)pyridin-2-yl]-2-propenoateHCID 22161738—

Reaction Conditions

Temperature100 °C

Reaction Steps

5.2 g of palladium(II) acetate, 77.8 g of potassium carbonate and 72.5 g of tetrabutylammonium bromide are added to a solution of 70 g of 3-benzyloxy-2-iodopyridine and 39.8 ml of acrylic acid methyl ester in 120 ml of dimethylformamide, and the suspension is stirred under argon atmosphere for 10 hours at 100° C. (bath temperature). The reaction mixture is concentrated by evaporation in a vacuum, the residue is added to water and shaken out with ethyl acetate. The organic phase is washed three times with water and once with saturated common salt solution, dried with sodium sulfate and concentrated by evaporation. The crude product is chromatographed on silica gel with hexane/10-25% ethyl acetate. 48.2 g of 3-(3-benzyloxy-2-pyridyl)-(2E)-2-propenoic acid methyl ester is obtained as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624943
Source datasetuspto-grants-1997_04
ORD IDord-d4846378d04a4d3fb9385b65082d0c14
Source noteuspto-grants-1997_04