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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethynyl-4-propylcyclohexane | HCID 21870626 | — |
| Reactant | 1-Bromo-4-ethoxy-2,3-difluorobenzene | HCID 26985491 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 1-Ethoxy-2,3-difluoro-4-(4-propylcyclohexylethynyl)benzene | HCID 19984524 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08945420B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-e76b039464e14f3dad843f034d8cb177 |
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| Source note | uspto-grants-2015_02 |
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