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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511482Generated: November 2, 2026

Potassium Phosphate, Tribasic → 1-(4-Ethoxy-2,3-difluorophenyl)-4-(4-ethoxy-2,3-difluorophenoxymethyl)-cyclohexane

https://huagongshe.com/reaction/1511482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Ethoxy-2,3-difluorophenolHCID 14495763—
Reactant4-Chloromethyl-(4-ethoxy-2,3-difluorophenyl)-cyclohexaneHCID 58058668—
SolventDimethylformamideHCID 6228—
Product1-(4-Ethoxy-2,3-difluorophenyl)-4-(4-ethoxy-2,3-difluorophenoxymethyl)-cyclohexaneHCID 6696248549.7%

Reaction Conditions

Temperature30 °C

Reaction Steps

4-Ethoxy-2,3-difluorophenol (6) (2.2 g) and tripotassium phosphate (K3PO4) (11.0 g) were added to DMF (100 ml) under a nitrogen atmosphere, and the stirring was continued at 70° C. The compound (20) (3.0 g) was added thereto, and the stirring was continued at 70° C. for 7 hours. After the reaction mixture obtained had been cooled to 30° C. and separated from the solid by filtration, toluene (100 ml) and water (100 ml) were added thereto and mixed. The mixture was then allowed to separate into organic and aqueous phases. The extraction into an organic phase was carried out. The organic phase obtained was washed with brine and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off, and the residue obtained was purified by means of column chromatography (silica gel/toluene=1/2 by volume). The product was further purified by means of recrystallization (Solmix A-11: heptane=1:2 by volume), giving 2.2 g of 1-(4-ethoxy-2,3-difluorophenyl)-4-(4-ethoxy-2,3-difluorophenoxymethyl)-cyclohexane (No. 828). The yield based on the compound (20) was 74.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08216489B2
Source datasetuspto-grants-2012_07
ORD IDord-ad66107672f441f194f23e7ba2397295
Source noteuspto-grants-2012_07