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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887697Generated: October 29, 2026

Carbon Dioxide → 3-Bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylic acid

https://huagongshe.com/reaction/887697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantSodium HydroxideHCID 14798—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-(3-Bromo-1H-pyrazol-1-yl)-3-chloropyridineHCID 21071278—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylic acidHCID 11587535—

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-(3-Bromo-pyrazol-1-yl)-3-chloro-pyridine (9.2 g) was dissolved in dry THF (80 mL) and cooled to −78° C. A solution of LDA (21.3 mL, 2.0 M) was added over a period of 10 min and stirred for further 15 min at −78° C. The solution was poured on crushed dry ice in THF (50 mL) and stirred for additional 1 h. Water and Et2O were added and 2N NaOH-solution was added to adjust the pH to 10-12. The layers were separated and the aqueous layer was washed 2× with Et2O and acidified with 2N HCl (pH ˜3). The resulting suspension was 3× extracted with MTB-ether, the combined org. layers were washed with brine, dried over MgSO4 and concentrated to afford 7.96 g of the title compound of the formula

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247431B2
Source datasetuspto-grants-2012_08
ORD IDord-93e6ab45751d42a197b6d720f7dd8007
Source noteuspto-grants-2012_08