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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Cyclopropanecarboxylic acid | HCID 15655 | — |
| Reactant | 2,3-Diethyl 2,3-pyridinedicarboxylate | HCID 10889517 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 6-Cyclopropylpyridine-2,3-dicarboxylic acid diethyl ester | HCID 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
| 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-61cddb36b2914d6ca7c820944a07ee2f |
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| Source note | uspto-grants-1991_03 |
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