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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Cyclopropanecarboxylic acid | HCID 15655 | — |
| Reactant | Diethyl 5-ethylpyridine-2,3-dicarboxylate | HCID 10857926 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Ethyl-6-cyclopropyl-pyridine-2,3-dicarboxylic acid | HCID 20067172 | 42.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04997947 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-8b16d12fa2e147f78b230a93275aa80d |
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| Source note | uspto-grants-1991_03 |
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