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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908882Generated: October 27, 2026

Potassium Iodide → {4'-[2-(Ethylthio)ethoxy]-2',6'-dimethylbiphenyl-3-yl}methanol

https://huagongshe.com/reaction/1908882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloroethyl ethyl sulfideHCID 12733—
Reactant3'-(Hydroxymethyl)-2,6-dimethylbiphenyl-4-olHCID 59342552—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product{4'-[2-(Ethylthio)ethoxy]-2',6'-dimethylbiphenyl-3-yl}methanolHCID 5934261447%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of 3′-(hydroxymethyl)-2,6-dimethylbiphenyl-4-ol (1.83 g, 8.00 mmol) and 2-chloroethyl ethyl sulfide (1.07 mL, 12.0 mmol) in N,N-dimethylformamide (15 mL) were added potassium carbonate (1.33 g, 9.60 mmol) and potassium iodide (0.132 g, 0.800 mmol), and the mixture was stirred at 95° C. for 24 hr under nitrogen atmosphere. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed successively with 1 M aqueous sodium hydroxide solution and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=10:90-50:50) to give the title compound (1.19 g, yield 47%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598226B2
Source datasetuspto-grants-2013_12
ORD IDord-ed8225f51f3e4033a43f0a83ebb35481
Source noteuspto-grants-2013_12