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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358847Generated: October 27, 2026

Carbon Dioxide → 5-Ethyl-6-cyclopropyl-pyridine-2,3-dicarboxylic acid

https://huagongshe.com/reaction/358847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantSulfuric AcidHCID 1118—
ReactantCyclopropanecarboxylic acidHCID 15655—
ReactantDiethyl 5-ethylpyridine-2,3-dicarboxylateHCID 10857926—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
Product5-Ethyl-6-cyclopropyl-pyridine-2,3-dicarboxylic acidHCID 2006717242.7%

Reaction Steps

There is added to a solution of 32 ml of concentrated sulphuric acid and 6.8 g of silver nitrate (AgNO3) in 400 ml of water first of all 50 g of 5-ethylpyridine-2,3-dicarboxylic acid diethyl ester and, when a homogeneous solution has been obtained, 25.8 g of cyclopropanecarboxylic acid. The solution is then heated to 70° and a solution of 68.2 g of ammonium peroxydisulphate (NH4)2S2O8 is added dropwise thereto while stirring vigorously. When the evolution of CO2 has ceased, the reaction mixture is stirred for a further 20 minutes, then cooled to 15° and extracted twice with 200 ml of methylene chloride each time. The methylene chloride extract is dried over magnesium sulphate, filtered and concentrated. The oily residue is purified by chromatography over a column of silica gel using ether/hexane 1:1. Evaporation of the solvent yields 20 g of 5-ethyl-6-cyclopropyl-pyridine-2,3-dicarboxylic acid in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04997947
Source datasetuspto-grants-1991_03
ORD IDord-8b16d12fa2e147f78b230a93275aa80d
Source noteuspto-grants-1991_03