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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593926Generated: November 1, 2026

Methane → Palladium

https://huagongshe.com/reaction/1593926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHydrochloric AcidHCID 313—
ReactantTriphenylphosphineHCID 11776—
ReactantBis(dibenzylideneacetone)palladiumHCID 9811564—
Reactant4-Bromo-3-phenyl-1H-pyrazoleHCID 178419463—
SolventTetrahydrofuranHCID 8028—
ProductPalladiumHCID 23938—
Product2'-(5-Ethyl-3,4-diphenyl-1H-pyrazol-1-yl)-[1,1'-biphenyl]-3-olHCID 27282214—

Reaction Steps

The reaction of Example 1 (reaction scale: 10 mmol of bromophenyl pyrazole) was conducted with 0.15 mole % of Pd2(dba)3. After the reaction was judged to be essentially complete, THF (10 mL/g of bromophenyl pyrazole starting material) was added to dissolve the precipitates, and the solution was passed through a Darco zeta pad twice. The filtrate was neutralized with 1N aq. HCl to a pH of 7.0 to 7.5. After filtration, the crude solid, whose palladium level was 111 ppm, was dissolved in THF (9 mL/g of bromophenyl pyrazole starting material), and the mixture was stirred in the presence of PS-PPh3 resin (Argonaut Technologies, 1.61 mmol PPh3/g, 5 wt %) at ambient temperature for 21 h, then filtered twice through a Darco zeta pad. The filtrate was concentrated and the product was recrystallized from THF/acetone/water to afford 2′-(5-ethyl-3,4-diphenyl-1H-pyrazol-1-yl)-[1,1′]-biphenyl-3-ol containing less than 2 ppm of palladium.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300639B2
Source datasetuspto-grants-2007_11
ORD IDord-79b9a0b8bf1346be8428627d02661132
Source noteuspto-grants-2007_11