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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358845Generated: October 30, 2026

Carbon Dioxide → 6-Cyclopropylpyridine-2,3-dicarboxylic acid diethyl ester

https://huagongshe.com/reaction/358845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantCyclopropanecarboxylic acidHCID 15655—
Reactant2,3-Diethyl 2,3-pyridinedicarboxylateHCID 10889517—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product6-Cyclopropylpyridine-2,3-dicarboxylic acid diethyl esterHCID 14280343—

Reaction Steps

40 g of pyridine-2,3-dicarboxylic acid diethyl ester are dissolved in a mixture of 400 g of water and 36 g of concentrated sulphuric acid and 6.1 g of silver nitrate (AgNO3). Subsequently, 32 g of cyclopropanecarboxylic acid are added and the reaction mixture is heated to 70°. A solution of 82.1 g of ammonium peroxydisulphate (NH4)2S2O8 in 300 ml of water is added dropwise thereto while stirring vigorously. When the evolution of CO2 has ceased, the reaction mixture is stirred for a further 20 minutes. It is then cooled to 15° and extracted twice with 200 ml of methylene chloride each time. The organic phase is collected, dried over magnesium sulphate, filtered and concentrated by evaporation. The residue is distilled at 13 millibars and the distillate is chromatographed over a column of silica gel with hexane/methylene chloride/ether. After the solvent has been evaporated 11.2 g of the above diester remain behind in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04997947
Source datasetuspto-grants-1991_03
ORD IDord-61cddb36b2914d6ca7c820944a07ee2f
Source noteuspto-grants-1991_03