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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1464782Erstellt: 26. Oktober 2026

Propargyl alcohol → (E)-6,6-dimethyl-4-hepten-2-yn-1-ol

https://huagongshe.com/reaction/1464782

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropargyl alcoholHCID 7859—
EduktButylamineHCID 8007—
EduktTriphenylphosphineHCID 11776—
Edukt(E)-1-iodo-3,3-dimethylbut-1-eneHCID 11063689—
KatalysatorPalladium ChlorideHCID 24290—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(E)-6,6-dimethyl-4-hepten-2-yn-1-olHCID 19917005—

Reaktionsschritte

0.63 g of (E)-1- iodo-3,3-dimethyl-1-butene [see J. Org. Chem., 43, 4424 (1978)] was dissolved in 10 ml of tetrahydrofuran, and 31 mg of triphenylphosphine, 29 mg of copper(I) iodide, 11 mg of palladium chloride, 1.5 ml of n-butylamine and 0.35 ml of propargyl alcohol were added. The mixture was stirred overnight at room temperature, and then water and ethyl acetate were added. The organic layer separated was worked up in a customary manner, and the product was purified by silica gel column chromatography [hexane/ethyl acetate=2/1] to give 0.27 g of the captioned compound as a pale brown oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05306728
Quelldatensatzuspto-grants-1994_04
ORD IDord-8bfc60aedb7d4839b58de804983eda20
Quellennotizuspto-grants-1994_04