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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDiisopropylamineHCID 7912—
Reactant3-FluoropyridineHCID 67794—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-Fluoropyridine-4-carboxylic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273764B2
Source datasetuspto-grants-2012_09
ORD IDord-ebf6f04e7079420e868b49b2430566b4
Source noteuspto-grants-2012_09