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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593923Generated: November 1, 2026

Hydrochloric Acid → Palladium

https://huagongshe.com/reaction/1593923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPalladiumHCID 23938—
ReactantBis(dibenzylideneacetone)palladiumHCID 9811564—
Reactant4-Bromo-3-phenyl-1H-pyrazoleHCID 178419463—
SolventAcetoneHCID 180—
SolventTetrahydrofuranHCID 8028—
ProductPalladiumHCID 23938—
Product2'-(5-Ethyl-3,4-diphenyl-1H-pyrazol-1-yl)-[1,1'-biphenyl]-3-olHCID 27282214—

Reaction Conditions

Temperature50 °C

Reaction Steps

The reaction of Example 1 (reaction scale: 10 mmol of bromophenyl pyrazole) was conducted with 0.1 mole % of Pd2(dba)3. After the reaction was judged to be essentially complete, the reaction mixture was neutralized with 1N aqueous HCl to a pH of 7.0 to 7.5. The crude product, whose palladium level was 270 ppm, was dissolved in acetone (16 mL/g of bromophenyl pyrazole starting material) and THF (2.65 mL/g) at 50° C. TMT (0.23 equiv.) was added, and the mixture was stirred at 50° C. for 15 min, cooled to room temperature, and filtered three times through a Darco zeta pad. A sample of filtrate was evaporated to dryness, affording a solid containing 92 ppm of palladium. The remaining filtrate was concentrated and recrystallized by adding water, affording 2′-(5-ethyl-3,4-diphenyl-1H-pyrazol-1-yl)-[1,1′]-biphenyl-3-ol containing 51 ppm of palladium.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300639B2
Source datasetuspto-grants-2007_11
ORD IDord-6d7f17ebd98c447d9d79f0afade30516
Source noteuspto-grants-2007_11