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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43356Generated: October 26, 2026

Methyl Acrylate → Ethyl (2E)-3-(5-formyl-2-pyridinyl)-2-propenoate

https://huagongshe.com/reaction/43356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantSodium AcetateHCID 517045—
Reactant6-Bromo-3-pyridinecarboxaldehydeHCID 11769234—
CatalystPalladium, di-mu-chlorobis(eta3-2-propenyl)di-HCID 61538—
SolventDimethylformamideHCID 6228—
ProductEthyl (2E)-3-(5-formyl-2-pyridinyl)-2-propenoateHCID 8662816093.7%

Reaction Conditions

Temperature170 °C

Reaction Steps

A mixture of 2-bromo-5-formylpyridine (500 mg, 2.6 mmol), methyl acrylate (0.6 ml, 6.5 mmol), tri-(o-tolyl)phosphine (80 mg, 0.26 mmol), allyl palladium (II) chloride dimer (47 mg, 0.13 mmol) and sodium acetate (1.08 g, 8 mmol) in DMF (10 ml) was heated at 170° C. in a microwave reactor for 0.75 h. The reaction mixture was filtered through Celite® then diluted with DCM and water. The organic phase was dried, concentrated in vacuo and purified by chromatography to give the title compound as a white solid (50 mg). δH (CDCl3, 250 MHz) 10.14 (1H, s), 9.09 (1H, d), 8.19 (1H, dd), 7.72 (1H, d), 7.57 (1H, d), 7.08 (1H, d), 3.85 (3H, s). MS (ES): MH+ 192.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536182B2
Source datasetuspto-grants-2013_09
ORD IDord-c0809180160c4ca9954d8ce9512a8b6f
Source noteuspto-grants-2013_09