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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212102Generated: October 31, 2026

Iodobenzene → HCID 69663474, compound

https://huagongshe.com/reaction/2212102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodobenzeneHCID 11575—
ReactantHCID 21048806HCID 21048806—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDiisopropylamineHCID 7912—
ProductHCID 69663474HCID 69663474—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1-(4-benzenesulfonyl-4-methylpentyl)-3-ethynylpiperidine (0.33 g, 1.0 mmol), iodobenzene (80 μL, 0.7 mmol), dichlorobis(triphenylphosphine)palladium(II) (35 mg, 0.05 mmol) and copper(I) iodide (6 mg, 0.03 mmol) in diisopropylamine (5 ml) was stirred at 70° C. for 2 hours. The reaction mixture was filtered through Celite, washing with dichloromethane (50 ml). The filtrate was concentrated in vacuo and the residue purified by flash column chromatography on silica gel, eluting with 2% methanol/dichloromethane, followed by an SCX cartridge and finally preparative thin layer chromatography, eluting with 7% methanol/dichloromethane, to give the title compound. The hydrochloride salt (63 mg, 14%) was obtained by treatment with ethereal hydrogen chloride and crystallisation from ethanol/diethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101892B2
Source datasetuspto-grants-2006_09
ORD IDord-f271806f0834401ebf6175ac5dd5a6fe
Source noteuspto-grants-2006_09