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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244842Generated: November 2, 2026

Hydrochloric Acid → 7,8-Difluoro-2-pentyl-5-(4-propylcyclohexylethynyl)chroman-6-ol

https://huagongshe.com/reaction/2244842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Ethynyl-4-propylcyclohexaneHCID 21870626—
Reactant7,8-Difluoro-5-iodo-2-pentylchroman-6-olHCID 59215257—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product7,8-Difluoro-2-pentyl-5-(4-propylcyclohexylethynyl)chroman-6-olHCID 59215268—

Reaction Steps

8.0 g (20.9 mmol) of 7,8-difluoro-5-iodo-2-pentylchroman-6-ol are stirred at 50° C. for 19 h together with 4.72 g (31.4 mmol) of 1-ethynyl-4-propylcyclohexane in the presence of 441 mg (0.63 mmol) of bis(triphenylphosphine)palladium(II) chloride and 120 mg (0.63 mmol) of copper(I) iodide in 90 ml of triethylamine. After cooling, the batch is added to ice/water and acidified using hydrochloric acid. The mixture is extracted a number of times with MTBE, and the combined extracts are washed with water and sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2, 1-chlorobutane). The phenol obtained is used directly for the following reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678929B2
Source datasetuspto-grants-2010_03
ORD IDord-3d18bb44540243279dc087295fe9109e
Source noteuspto-grants-2010_03