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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081625Generated: October 25, 2026

1-Iodonaphthalene → 5-(1-Naphthyl)-4-pentyn-1-ol

https://huagongshe.com/reaction/1081625

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodonaphthaleneHCID 7004—
Reactant4-Pentyn-1-olHCID 79346—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDiethylamineHCID 8021—
Product5-(1-Naphthyl)-4-pentyn-1-olHCID 1995555768.7%

Reaction Steps

Under a nitrogen atmosphere, a mixture of 4.0 mL (0.027 mole) of 1-iodonaphthalene, 0.1 gram (0.0003 mole) of copper(I) iodide, and 0.19 gram (0.0003 mole) of bis(triphenylphosphine)palladium(II) chloride in 75 mL of diethylamine was stirred, and 2.6 mL (0.027 mole) of 4-pentyn-1-ol was added in one portion. Upon completion of addition, the reaction mixture was stirred at ambient temperature for about 18 hours. Gas chromatographic (GC) analysis of the reaction mixture indicated that the reaction had not gone to completion. An additional 0.5 mL of the 4-pentyn-1-ol was added, and the reaction mixture was stirred for an additional six hours. GC analysis of the reaction mixture indicated that the reaction was complete. The reaction mixture was passed through a column of silica gel. Elution was accomplished using methylene chloride. The eluate was concentrated under reduced pressure, yielding 3.9 grams of 5-(naphth-1-yl)-4-pentyn-1-ol. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587379
Source datasetuspto-grants-1996_12
ORD IDord-560e4079e4974c14a8836363b0fa61dc
Source noteuspto-grants-1996_12