Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2271653Erstellt: 26. Oktober 2026

Trimethylsilylacetylene → 3-Nitro-5-((trimethylsilyl)ethynyl)pyridine

https://huagongshe.com/reaction/2271653

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilylacetyleneHCID 66111—
Edukt3-Bromo-5-nitropyridineHCID 2762898—
KatalysatorCopper iodideHCID 83717—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTriethylamineHCID 8471—
Produkt3-Nitro-5-((trimethylsilyl)ethynyl)pyridineHCID 66715702159,3%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a suspension of 3-bromo-5-nitropyridine (1.0 g, 4.90 mmol), Pd(Ph3P)4 (0.57 g, 0.49 mmol), and copper iodide (0.19 g, 0.98 mmol) in triethylamine (30 mL) was added ethynyltrimethylsilane (1.0 mL, 7.35 mmol) and the reaction was purged with N2. The mixture was stirred at 80° C. for 2 h. The reaction mixture was filtered through celite and washed with ethyl acetate. The filtrate was washed with saturated solutions of NaHCO3 and NaCl. The organic layer was concentrated to afford the crude product (1.72 g) as a light brown solid: ESI MS m/z 221 [C10H12N2O2Si+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09120749B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-ca7f18693e3641b992c4d5a3cef535c2
Quellennotizuspto-grants-2015_09