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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 76864Erstellt: 24. Oktober 2026

Methanol → Benzonitrile, m-chloro-

https://huagongshe.com/de/reaction/76864

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktDiethylamineHCID 8021—
Edukt4-(Bromomethyl)-3-chlorobenzonitrileHCID 13042093—
Edukt4-(2-((tert-Butyldimethylsilyl)oxy)ethyl)-1-trityl-1H-imidazoleHCID 66885359—
LösungsmittelAcetonitrileHCID 6342—
ProduktBenzonitrile, m-chloro-HCID 13015—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

4-[2-(tert-Butyldimethylsilanyloxy)ethyl]-1-trityl-1H-imidazole (3.98 g, 8.5 mmol) and 4-bromomethyl-3-chlorobenzonitrile (2.93 g, 12.7 mmol) are dissolved in MeCN (40 mL) and heated at 80° C. for 5 h. After cooling to room temperature MeOH (40 mL) and Et2NH (7 mL) are then added and the solution is warmed 70° C. for 1 h. The solution is evaporated to dryness and the residue purified via flash column chromatography (acetone/CH2Cl2 1:3→MeOH/CH2Cl2 5:95) to give 4-{5-[2-tert-butyl-dimethylsilanyloxy)ethyl]-imidazol-1-ylmethyl}-3-chlorobenzonitrile as an oil. MS (ESI) m/z 376.3, 378.3 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835646B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-79cdbd8def654cd999b2d85bcce979ca
Quellennotizuspto-grants-2014_09