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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857606Generated: October 26, 2026

Water → HCID 21869386, compound

https://huagongshe.com/reaction/857606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
Reactant(4-Propylphenoxy)boronic acidHCID 21869456—
Reactant1,3-Difluoro-2-trifluoromethoxynaphthalene-6-yl trifluoromethanesulfonateHCID 54265538—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductHCID 21869386HCID 2186938661.9%

Reaction Conditions

Temperature85 °C

Reaction Steps

7.3 g of 4-propylphenylboric acid and 11 g of 1,3-difluoro-2-trifluoromethoxynaphthalene-6-yl trifluoromethanesulfonate (obtained by triflating 1,3-difluoro-2-trifluoromethoxynaphthalene-6-ol with trifluoromethanesulfonic anhydride) were dissolved in 50 ml of DMF. To the solution was then added 0.4 g of tetrakis(triphenylphosphine)palladium (0). The reaction mixture was stirred at a temperature of 85° C. for 8 hours. To the reaction solution were then added water and toluene. The resulting aqueous phase was then extracted with toluene. The material thus extracted and the organic phase were together washed with water and then with saturated brine, and then dried over anhydrous sodium sulfate. The solvent was then distilled off under reduced pressure to obtain an oily matter. The oily matter thus obtained was purified through silica gel column chromatography (hexane/ethyl acetate=9/1), and then recrystallized from ethanol to obtain 6.3 g of 1,3-difluoro-2-trifluoromethoxy-6-(4-propylphenyl)naphthalene in crystal form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07145047B2
Source datasetuspto-grants-2006_12
ORD IDord-f5e2dc8a695c4b818a99dc3fdbf456e9
Source noteuspto-grants-2006_12