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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593922Generated: October 31, 2026

Hydrochloric Acid → Palladium

https://huagongshe.com/reaction/1593922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantBis(dibenzylideneacetone)palladiumHCID 9811564—
Reactant4-Bromo-3-phenyl-1H-pyrazoleHCID 178419463—
SolventWaterHCID 962—
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 0.5 mole % of Pd2(dba)3. After the reaction was judged to be essentially complete, 5N aqueous HCl (1.25 mL/g of bromophenyl pyrazole starting material) was added followed by THF (12.5 mL/g) and water (2.5 mL/g). The mixture was heated to 50° C. to dissolve the precipitates, then cooled to 25° C. and filtered twice through a Darco zeta pad. To the filtrate was added TMT (5 mol %). The mixture was stirred at ambient temperature for 14 h and filtered again four times through the same Darco zeta pad employed in the previous filtration. The THF was removed by evaporation, and water (2.5 mL/g) and ethanol (2.5 mL/g) were added to precipitate the product, affording 2′-(5-ethyl-3,4-diphenyl-1H-pyrazol-1-yl)-[1,1′]-biphenyl-3-ol containing 146 ppm of palladium.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300639B2
Source datasetuspto-grants-2007_11
ORD IDord-1bc14417357d40998db9ebcb82d41929
Source noteuspto-grants-2007_11