Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509578Generated: October 25, 2026

Ethanol → Ethyl 5-ethoxypyridine-2-carboxylate

https://huagongshe.com/reaction/509578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodiumHCID 5360545—
ReactantEthyl 5-bromopicolinateHCID 12686158—
ProductEthyl 5-ethoxypyridine-2-carboxylateHCID 67958698—

Reaction Steps

To a solution of ethyl 5-bromopyridine-2-carboxylate 2 (1.5 g, 6.5 mmol) in 20 mL of EtOH was added a solution of sodium (0.18 g, 7.8 mmol) in 20 mL of EtOH. The mixture was stirred at reflux for 3 h. After removal of all solvent, the residue was purified by column (2:1 of hexane/ethyl acetate) to give ethyl 5-ethoxypyridine-2-carboxylate 3 as an oil. Yield: 0.26 g, 20%. 1HNMR (CDCl3) δ (ppm): 8.38 (d, 1 H), 8.10 (d, 1 H), 8.23 (d, 1 H), 7.22 (dd, 1 H), 4.45 (m, 2 H), 4.25 (m, 1 H), 1.40 (m, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096587B2
Source datasetuspto-grants-2015_08
ORD IDord-616a54581dc044c5986ac7ee96772b3f
Source noteuspto-grants-2015_08