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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 28372Erstellt: 25. Oktober 2026

Trimethylsilylacetylene → 1-(2-Bromo-5-fluorophenyl)-4-(trimethylsilyl)-1H-1,2,3-triazole

https://huagongshe.com/reaction/28372

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilylacetyleneHCID 66111—
Edukt2-Azido-1-bromo-4-fluorobenzeneHCID 21069825—
LösungsmittelTolueneHCID 1140—
Produkt1-(2-Bromo-5-fluorophenyl)-4-(trimethylsilyl)-1H-1,2,3-triazoleHCID 2106977095,2%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A mixture of 2-azido-1-bromo-4-fluorobenzene (1.047 g, 4.85 mmol) and trimethylsilylacetylene (2.01 mL, 14.54 mmol) in toluene (5 mL) was heated in a pressure vessel at 110° C. for 21.5 h. The reaction mixture was concentrated in vacuo and the residue was purified with a Biotage system on silica gel with hexanes:ethyl acetate (9:1) gradient as the eluent to afford the title compound as a colorless oil (1.451 g, 95% yield): 1H NMR (400 MHz, CDCl3) o ppm: 7.97 (1H, s), 7.74 (1H, dd, J=9.0, 5.4 Hz), 7.37 (1H, dd, J=8.5, 2.9 Hz), 7.16 (1 H, ddd, J=8.8, 7.6, 3.0 Hz), 0.40 (9 H, s), LCMS (+ESI, M+H+) m/z 314/316.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07419969B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-5332d1e5adb14dd9a07ded2609a8182b
Quellennotizuspto-grants-2008_09