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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755Generated: October 25, 2026

Ethyl Acrylate → Ethyl 3-{3-hydroxy-6-hydroxymethylpyridin2-yl}propenoate

https://huagongshe.com/reaction/1755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantTriphenylphosphineHCID 11776—
ReactantPotassium AcetateHCID 517044—
Reactant3-Hydroxy-6-hydroxymethyl-2-iodopyridineHCID 19692709—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-{3-hydroxy-6-hydroxymethylpyridin2-yl}propenoateHCID 54362899—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 3-hydroxy-6-hydroxymethyl-2-iodopyridine (708 mg, 2.82 mmol) in DMF (5.7 ml) and water (0.3 ml) were added potassium acetate (0.74 g, 7.5 mmol), triphenylphosphine (63 mg, 0.24 mmol), ethyl acrylate (0.98 ml, 0.90 g, 9.0 mmol) and palladium acetate (27 mg, 0.12 mmol). The mixture was placed under nitrogen and stirred and heated at 120° C. for 5 h. The mix was cooled and poured into water (50 ml). The product was extracted into ethyl acetate (3×20 ml) and the combined extracts were washed with water (2×15 ml) with brine (15 ml), dried and evaporated. The etude product was purified by passage in ethyl acetate through a pad of silica, yielding after evaporation a yellow solid (295 g, 47%). mp (B.HCl) 199°-203° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726315
Source datasetuspto-grants-1998_03
ORD IDord-33f5c2c61cec497c9cae12b9bafc104f
Source noteuspto-grants-1998_03