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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841829Generated: November 2, 2026

1-Ethynyl-4-propylcyclohexane → 1-Ethoxy-2,3-difluoro-4-(4-propylcyclohexylethynyl)benzene

https://huagongshe.com/reaction/1841829

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethynyl-4-propylcyclohexaneHCID 21870626—
Reactant1-Bromo-4-ethoxy-2,3-difluorobenzeneHCID 26985491—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventHydrochloric AcidHCID 313—
SolventTriethylamineHCID 8471—
Solventtert-Butyl methyl etherHCID 15413—
Product1-Ethoxy-2,3-difluoro-4-(4-propylcyclohexylethynyl)benzeneHCID 19984524—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 20.6 g (0.14 mol) of 1-ethynyl-4-propylcyclohexane, 25.0 g (0.11 mol) of 1-bromo-4-ethoxy-2,3-difluorobenzene, 2.22 g (3.16 mmol) of bis(triphenylphosphine)palladium(II) chloride and 603 mg (3.16 mmol) of copper(I) iodide in 440 ml of triethylamine is warmed at 50° C. for 19 h. After cooling, the mixture is diluted with MTBE and neutralised using dil. hydrochloric acid. The organic phase is separated off, and the aqueous phase is extracted with MTBE. The combined organic phases are washed with sodium chloride solution and dried using sodium sulfate. The solution is concentrated to dryness, and the residue is purified by column chromatography (SiO2, n-heptane:chlorobutane=9:1). The further purification is carried out by recrystallisation from n-heptane, giving 1-ethoxy-2,3-difluoro-4-(4-propylcyclohexylethynyl)benzene as a colourless solid (m.p. 64° C.). This has the phase sequence: C 64° C. I. The properties, extrapolated from a 10% solution in ZLI-4792, are:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08945420B2
Source datasetuspto-grants-2015_02
ORD IDord-e76b039464e14f3dad843f034d8cb177
Source noteuspto-grants-2015_02