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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1916707Erstellt: 26. Oktober 2026

Trimethylsilylacetylene → 2-(5-Trimethylsilanylethynyl-indol-1-yl)-ethanol

https://huagongshe.com/reaction/1916707

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilylacetyleneHCID 66111—
Edukt2-(5-Iodo-indol-1-yl)-ethanolHCID 45789380—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelTriethylamineHCID 8471—
Produkt2-(5-Trimethylsilanylethynyl-indol-1-yl)-ethanolHCID 67364573—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

398 mg (2.1 mmol) CuI and 1.47 g (2.1 mmol) Pd(PPh3)2Cl2 are added to a solution, cooled to 0° C., of 30 g (104 mmol) 2-(5-iodo-indol-1-yl)-ethanol and 18 mL (125 mmol) ethynyl-trimethyl-silane in 480 mL triethylamine and 120 mL THF and stirred for 30 min at 0° C. and 2 h at RT. The mixture is evaporated down i. vac., the residue is taken up in 300 mL EtOAc, the organic phase is washed with 150 mL water and dried over Na2SO4. After the desiccant and solvent have been eliminated the residue is purified by chromatography (silica gel, gradient: cyc/EtOAc 4:1 to 2:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08618132B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-5f39630562004788afc88eab2ed230ba
Quellennotizuspto-grants-2013_12