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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2165532Erstellt: 25. Oktober 2026

Trimethylsilyl cyanide → HCID 15176140, Verbindung

https://huagongshe.com/reaction/2165532

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilyl cyanideHCID 82115—
Edukt1-Azabicyclo(3.3.1)nonan-4-oneHCID 417897—
Katalysatorzinc(II)iodideHCID 9883512—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 15176140HCID 15176140—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Trimethylsilyl cyanide (3 ml) was added dropwise to a stirred solution of 1-azabicyclo[3.3.1]nonan-4-one (2.5 g) and zinc iodide (0.15 g) in dry dichloromethane (20 ml) and the resulting mixture was heated at reflux for 4 hours. The mixture was cooled and the solvent removed at reduced pressure; the residue was dissolved in dry tetrahydrofuran (20 ml) and cooled to 0° C. A solution of lithium aluminium hydride in tetrahydrofuran (18 ml of 1.0M soln) was then added and the resulting solution stirred overnight at room temperature. Water (0.7 ml), followed by 15% sodium hydroxide (aq) (0.7 ml) and water (2.1 ml) were then added and the precipitate removed by filtration. Evaporation of the filtrate yielded the title compound (2.2 g); δH (360 MHz, CDCl3) 1.2-1.3 (2H, m, CH2), 1.34 (1H, m, CHH), 1.41 (1H, m, CHH), 1.6 (2H, m, CH2), 1.7-1.74 (1H, m, CHH), 1.76-1.91 (2H, m, CH2), 2.11-2.16 (1H, m, CHH), 2.67-3.18 (8H, m); m/z 170 (M+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04940703
Quelldatensatzuspto-grants-1990_07
ORD IDord-3216517382fb49deaa2acd4da1c4f945
Quellennotizuspto-grants-1990_07