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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1166093Erstellt: 24. Oktober 2026

Propargyl alcohol → 3-[4-(1h-Pyrazol-1-yl)phenyl]-2-propyn-1-ol

https://huagongshe.com/reaction/1166093

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropargyl alcoholHCID 7859—
Edukt1-(4-bromophenyl)-1H-pyrazoleHCID 10443564—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
Produkt3-[4-(1h-Pyrazol-1-yl)phenyl]-2-propyn-1-olHCID 2263092537%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 1-(4-bromophenyl)-1H-pyrazole (prepared as described in Bull. Soc. Chim. Fr. 1966, 2832) (2.24 g, 10.04 mmol), Pd(Ph3P)2Cl2 (180 mg, 0.26 mmol), and copper(I) iodide (95 mg, 0.50 mmol) in TEA (20 mL) was stirred for 5 min, propargyl alcohol (0.70 mL, 12.02 mmol) was added, and the mixture was heated to 80° C. for 48 h. The volatiles were evaporated, ethyl acetate (50 mL) and water (50 mL) were added to the residue, and the mixture was filtered through a pad of Celite. The organic layer from the filtrate was washed with brine (50 mL), dried (Na2SO4), and concentrated. Purification by chromatography (SiO2, 3:2 hexane/ethyl acetate) yielded 0.73 g (37%) of the title compound as a brown solid. MS 199 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06613747B2
Quelldatensatzuspto-grants-2003_09
ORD IDord-7c861f51a31c4e799360860a92b4a99d
Quellennotizuspto-grants-2003_09