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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733127Generated: October 25, 2026

Citric Acid → 5-tert-butyl-1-(2'-chloro-1,1'-biphenyl-3-yl)-1H-pyrazole-3-carboxylic acid

https://huagongshe.com/reaction/733127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chlorophenylboronic acidHCID 2734322—
Reactantethyl 1-(3-bromophenyl)-5-tert-butyl-1H-pyrazole-3-carboxylateHCID 57428253—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Solvent1-PropanolHCID 1031—
Product5-tert-butyl-1-(2'-chloro-1,1'-biphenyl-3-yl)-1H-pyrazole-3-carboxylic acidHCID 11279690—

Reaction Steps

To a solution of ethyl 1-(3-bromophenyl)-5-tert-butyl-1H-pyrazole-3-carboxylate and 2-chlorophenylboronic acid (0.279 g, 1.78 mmol) in n-propanol:water (2.35 ml:0.482 ml) mixture were added palladium acetate (0.005 g), triphenylphosphine (0.016 g) and 2N sodium carbonate (0.497 ml) and the solution was refluxed for 16 hours. To the reaction, a 2N solution of NaOH (1.5 ml) was added and refluxed for an additional 2 hours. The solution was cooled, acidified with 10% citric acid and extracted into ethyl acetate. The organic phase was washed with brine, dried over sodium sulfate, filtered and concentrated to give 0.212 g of 5-tert-butyl-1-(2′-chloro-1,1′-biphenyl-3-yl)-1H-pyrazole-3-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589116B2
Source datasetuspto-grants-2009_09
ORD IDord-3b54fcb58b5f418dbddf2a237380cde7
Source noteuspto-grants-2009_09