HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390486Generated: October 30, 2026
Carbon Dioxide → 3-Fluoropyridine-4-carboxylic acid
https://huagongshe.com/reaction/2390486
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 3-Fluoropyridine | HCID 67794 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-Fluoropyridine-4-carboxylic acid | HCID 345361 | — |
Reaction Steps
To a mixture of 39.9 ml of diisopropylamine and 257 ml of tetrahydrofuran was added 107 ml of a 2.64 M hexane solution of n-butyllithium under stirring while cooling the mixture in a dry ice-acetone bath, then, the mixture was stirred for 1.5 hours. Then, 25.0 g of 3-fluoropyridine was added, and the mixture was further stirred for 1.5 hours. Crushed dry ice was added to the reaction mixture, then, cooling was stopped, and the mixture was stirred until returning to room temperature. Water was added, and most of hexane and tetrahydrofuran were distilled off under reduced pressure. The residue was washed with tert-butyl methyl ether, and the aqueous layer was recovered. To the resultant aqueous layer was added concentrated hydrochloric acid under ice cool, and pH of the mixture was adjusted to 3 and the mixture was stirred for 1 hour. The deposit was collected by filtration, and dried under reduced pressure to obtain 32.51 g of 3-fluoroisonicotinic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273764B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-ebf6f04e7079420e868b49b2430566b4 |
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| Source note | uspto-grants-2012_09 |
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