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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19782Erstellt: 25. Oktober 2026

Trimethylsilylacetylene → 2-Chloro-4-(2-(trimethylsilyl)ethynyl)pyridine

https://huagongshe.com/reaction/19782

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilylacetyleneHCID 66111—
Edukt4-Bromo-2-chloropyridineHCID 3847770—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorDichlorobis(triphenylphosphine)palladiumHCID 6102075—
LösungsmittelTriethylamineHCID 8471—
Produkt2-Chloro-4-(2-(trimethylsilyl)ethynyl)pyridineHCID 2198539191%

Reaktionsschritte

A mixture of 2.5 g of 4-bromo-2-chloropyridine (12.6 mmol), 2.2 ml of (trimethylsilyl)acetylene (15.1 mmol), 153 mg of copper(I)iodide (0.79 mmol) and 287 mg of bis(triphenylphosphine)palladium(II)chloride (0.41 mmol) in triethylamine (15 ml) was stirred at RT for 1 h. The triethylamine was then removed in vacuo, water was added and the mixture was extracted with diethylether. The combined organic extracts were then washed with water and brine, dried (Na2SO4), filtered and concentrated in vacuo to give a residue which was purified by column chromatography (heptane/EtOAc 100:0 to 98:2) to give 2-chloro-4-trimethylsilanylethynyl-pyridine (2.394 g, 91%) as a light yellow liquid. MS (ISP) 210.1 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745477B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-42fbcf0d962848b08f31746a54c93e2b
Quellennotizuspto-grants-2010_06