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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070040Generated: October 31, 2026

Hydrochloric Acid → Ethyl oxo(pyridin-3-yl)acetate

https://huagongshe.com/reaction/1070040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl OxalateHCID 7268—
Reactant3-BromopyridineHCID 12286—
ReactantSodium BicarbonateHCID 516892—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventEthyl acetate hexaneHCID 21226206—
ProductEthyl oxo(pyridin-3-yl)acetateHCID 1248770545%

Reaction Conditions

Temperature0 °C

Reaction Steps

n-Butyllithium (1.6N hexane solution, 108 ml) was added dropwise to a diethyl ether solution (400 ml) of 3-bromopyridine (25.7 g) at −78° C. over 1 hour under nitrogen atmosphere. After stirring for 30 minutes, a diethyl ether solution (100 ml) of diethyl oxalate (28.6 g) was added dropwise thereto at −78° C. over 1 hour. The reaction mixture was further mixed for 30 minutes, allowed to warm to 0° C., and 1N hydrochloric acid (200 ml) was added thereto. After stirring for 30 minutes, sodium bicarbonate was added thereto to neutralize the reaction mixture. The organic layer was separated, washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was subjected to silica gel chromatography to obtain ethyl 3-pyridylglyoxylate (13.1 g, yield 45%) from an ethyl acetate-hexane (1:1, v/v)-eluted fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251926B1
Source datasetuspto-grants-2001_06
ORD IDord-f612db15822a4201ba95bf86361da92c
Source noteuspto-grants-2001_06