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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 440950Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/440950

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-IodonaphthaleneHCID 7004—
Edukt4-Pentyn-1-olHCID 79346—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelDiethylamineHCID 8021—
Produkt5-(1-Naphthyl)-4-pentyn-1-olHCID 1995555768,7%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05521192
Quelldatensatzuspto-grants-1996_05
ORD IDord-0e2091d86477426185264f1752389d97
Quellennotizuspto-grants-1996_05