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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754Generated: October 26, 2026

Ethyl Acrylate → Ethyl (3-hydroxy-6-methylpyridin-2-yl)propenoate

https://huagongshe.com/reaction/1754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantTriphenylphosphineHCID 11776—
Reactant2-Iodo-6-methylpyridin-3-olHCID 89957—
ReactantPotassium AcetateHCID 517044—
CatalystPalladium ChlorideHCID 24290—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl (3-hydroxy-6-methylpyridin-2-yl)propenoateHCID 131720091—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 3-hydroxy-2-iodo-6-methylpyridine (1.175 g, 5.0 mmol) in DMF (9.5 ml) and water (0.5 ml) were added potassium acetate (1.23 g, 12.5 mmol), triphenylphosphine (105 mg, 0.40 mmol), palladium chloride (36 mg, 0.20 mmol) and ethyl acrylate (1.63 ml, 1.50 g, 15.0 mmol). The mixture was placed under nitrogen and heated at 120° C. for 1.5 h. The mixture was cooled, filtered from deposited palladium black, and added to water (100 ml). The product was extracted into ethyl acetate (3×30 ml). The combined extracts were washed with water (2×25 ml) and with brine (25 ml), then dried over sodium sulphate and evaporated. This left a tan solid, the product (951 mg, 91%). mp 192°-195° C. (dec)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726315
Source datasetuspto-grants-1998_03
ORD IDord-daea2679130c4e96a69efc91647c4537
Source noteuspto-grants-1998_03