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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509769Generated: October 30, 2026

Sodium metaborate → 4-[(3,5-Difluoro-4-trifluoromethylphenoxy)difluoromethyl]-4'-(4-ethylcyclohexyl)-3,5,2'-trifluorobiphenyl

https://huagongshe.com/reaction/1509769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium metaborateHCID 145326—
ReactantCID 22602656HCID 22602656—
ReactantHCID 58444567HCID 58444567—
Reactant4-(4-Ethylcyclohexyl)-2-fluorophenylboronic acidHCID 58444591—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-[(3,5-Difluoro-4-trifluoromethylphenoxy)difluoromethyl]-4'-(4-ethylcyclohexyl)-3,5,2'-trifluorobiphenylHCID 58444585—

Reaction Steps

0.11 ml (2.33 mmol) of hydrazine hydroxide is added to a mixture of 9.70 g (22.1 mmol) of 5-((4-bromo-2,6-difluorophenyl)difluoromethoxy)-1,3-difluoro-2-(trifluoromethyl)benzene, 12 ml (18 mmol) of 1.5 N aqueous sodium metaborate soln. and 0.62 g (0.88 mmol) of bis(triphenylphosphine)palladium(II) chloride in 150 ml of THF at room temperature. 6.1 g (24.3 mmol) of 4-(4-ethylcyclohexyl)-2-fluorobenzeneboronic acid are added, and the mixture is heated at the boil for 18 h. After cooling, water is added, and the batch is extracted with MTBE. The aqueous phase is extracted with MTBE, and the combined organic phases are washed with water and saturated sodium chloride solution. The solution is dried using sodium sulfate and concentrated to dryness. The crude product is purified by column chromatography (SiO2, n-heptane:1-chlorobutane=9:1). The further purification is carried out by recrystallisation from ethanol and n-heptane, giving 4-[(3,5-difluoro-4-trifluoromethylphenoxy)difluoromethyl]-4′-(4-ethylcyclohexyl)-3,5,2′-trifluorobiphenyl as a colourless solid having an m.p. of 77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211513B2
Source datasetuspto-grants-2012_07
ORD IDord-a863bf41bcca43c5804a8746830b960f
Source noteuspto-grants-2012_07