Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691518Generated: November 2, 2026

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

https://huagongshe.com/reaction/1691518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantEthane, 1-chloro-2-ethoxy-HCID 12341—
Reactant4'-Hydroxy-2',6'-dimethyl-[1,1'-biphenyl]-3-carbaldehydeHCID 23111691—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4'-(2-Ethoxyethoxy)-2',6'-dimethylbiphenyl-3-carbaldehydeHCID 2311172289%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4′-hydroxy-2′,6′-dimethylbiphenyl-3-carbaldehyde (8.52 g, 37.7 mmol) and 2-chloroethyl ethyl ether (6.15 g, 56.6 mmol) in N,N-dimethylformamide (40 mL) were added potassium carbonate (6.25 g, 45.2 mmol) and potassium iodide (1.25 g, 7.54 mmol), and the mixture was stirred at 80° C. for 18 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=5:95-25:75) to give the title compound (10.0 g, yield 89%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153694B2
Source datasetuspto-grants-2012_04
ORD IDord-2071af67b9454429bf11ece6e5bcf279
Source noteuspto-grants-2012_04