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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273381Generated: October 31, 2026

Potassium Iodide → 4'-(Methoxymethoxy)-2',6'-dimethylbiphenyl-3-carbaldehyde

https://huagongshe.com/reaction/273381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantPotassium CarbonateHCID 11430—
Reactant4'-Hydroxy-2',6'-dimethyl-[1,1'-biphenyl]-3-carbaldehydeHCID 23111691—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4'-(Methoxymethoxy)-2',6'-dimethylbiphenyl-3-carbaldehydeHCID 2315730632%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 4′-hydroxy-2′,6′-dimethylbiphenyl-3-carbaldehyde (4.5 g, 19.9 mmol), chloromethyl methyl ether (2.3 mL, 30.3 mmol), potassium carbonate (5.5 g, 39.8 mmol) and potassium iodide (0.66 g, 3.98 mmol) in N,N-dimethylformamide (50 mL) was stirred at 70° C. for 20 hrs. The reaction solution was diluted with ethyl acetate, washed successively with aqueous citric acid solution, water and saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate:hexane=3:97-1:9) to give the title compound (1.7 g, yield 32%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456218B2
Source datasetuspto-grants-2008_11
ORD IDord-2219d23b38734d67b4878eba4edc2006
Source noteuspto-grants-2008_11