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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511486Generated: October 26, 2026

Potassium Phosphate, Tribasic → HCID 178450201, compound

https://huagongshe.com/reaction/1511486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Butoxy-2,3-difluorophenolHCID 19103433—
Reactant4-Chloromethyl-(4-ethoxy-2,3-difluorophenyl)-cyclohexaneHCID 58058668—
SolventDimethylformamideHCID 6228—
ProductHCID 178450201HCID 17845020185.1%

Reaction Conditions

Temperature30 °C

Reaction Steps

4-Butoxy-2,3-difluorophenol (24) (4.6 g) and tripotassium phosphate (K3PO4) (14.0 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 solid materials 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, and 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; heptane/toluene=1/2 by volume). The product was further purified by means of recrystallization (Solmix A-11: heptane=1:2 by volume), giving 4.02 g of 2,3-difluoro-4-ethoxy-[trans-4-(2,3-difluoro-4-butoxyphenoxymethyl)cyclohexyl]benzene (No. 831). The yield based on the compound (20) was 85.1%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08216489B2
Source datasetuspto-grants-2012_07
ORD IDord-b1248a9b30144ebe803f7c1c7576bd3c
Source noteuspto-grants-2012_07