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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411284Generated: October 30, 2026

Triethylamine → Ethyl 3-(2-methoxypyrimidin-5-yl)acrylate

https://huagongshe.com/reaction/411284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcrylateHCID 8821—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantPyrimidine, 5-bromo-2-methoxy-HCID 139657—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
ProductEthyl 3-(2-methoxypyrimidin-5-yl)acrylateHCID 53940995—

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of 2-methoxy-5-bromopyrimidine (75.43 g, 0.399 mol), ethyl acrylate (47.5 ml, 0.439 mol), palladium (II) acetate (1.07 g, 0.0048 mol), tri-o-tolylphosphine (2.92 g, 0.0096 mol) and triethylamine (84 ml) were heated at 135° C. with stirring under argon for 12 h. After allowing to cool the solid mass was dissolved in water and ethyl acetate, filtered, and the aqueous phase separated and further extracted with ethyl acetate. The combined extracts were washed with saturated aqueous ammonium chloride, dried (MgSO4) and evaporated. The solid thus obtained was triturated with ether/light petrol (1:3, 350 ml), filtered, washed and dried, yield 52.41 g (63%). 1H-NMR (CDCl3) δ1.33 (3H, t), 4.06 (3H, s), 4.28 (2H, q), 6.45 (1H, d), 7.58 (1H, d), 8.67 (2H, s); MS (APCI+) found (M+H)=209; C10H12N2O3 requires 208.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559155B1
Source datasetuspto-grants-2003_05
ORD IDord-f2201ad1ea8c474b8e7779e2c2ba7bd7
Source noteuspto-grants-2003_05