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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786730Generated: October 30, 2026

Trimethylphosphine → 4-Methoxybiphenyl

https://huagongshe.com/reaction/1786730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylphosphineHCID 68983—
ReactantHCID 10856767HCID 10856767—
CatalystNickelHCID 935—
CatalystNickel(II) acetylacetonateHCID 9834912—
Product4-MethoxybiphenylHCID 119431,600%

Reaction Steps

The procedure was identical to Example 1, with the exception that the nickel catalyst used was derived in situ from a combination of anhydrous nickel acetylacetonate (0.026 g; 5 mol %) and trimethylphosphine (0.20 mL of 1 M solution in toluene; 10 mol %). GC analysis of the organic phase of the hydrolyzed reaction sample after 2 h at 60° C. showed the presence of 1.76 mmol (88% yield) of 4-phenylanisole, 0.11 mmol of 4-methoxybenzophenone imine, and no remaining 4-methoxybenzonitrile in the reaction mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507830B2
Source datasetuspto-grants-2009_03
ORD IDord-e718b5c472454dc0b21020ceafb9ad37
Source noteuspto-grants-2009_03