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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 264096Erstellt: 26. Oktober 2026

1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde → HCID 54381600, Verbindung

https://huagongshe.com/reaction/264096

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
EduktTriphenylundecylphosphonium bromideHCID 3085198—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 54381600HCID 5438160064%

Reaktionsschritte

A solution of n-BuLi (4.1 mL, 6.5 mmol, 1.6M in hexanes) was added dropwise to a suspension of n-undecyl-triphenylphosphoniumbromide (3.09 g, 6.2 mmol, obtained from triphenylphosphine and undecylbromide) in 100 mL THF at -78° C. under an atmosphere of N2. The resulting orange solution was stirred for 45 minutes before a solution of 1-(triphenylmethyl)-4-imidazolecarboxaldehyde (2.0 g, 5.9 mmol, Ref: Kelly J. L., Miller C. A., and McLean E. W., J. Med. Chem. 1977;20:721) in 75 mL THF was added dropwise. Warmed to room temperature and stirred for 16 hours. Quenched by adding 50 mL saturated NH4Cl solution and concentrating in vacuo. The residue was partitioned between water and dichloromethane. The organic layer was dried over MgSO4, filtered, and concentrated to give a yellow oil. Chromatography (10% EtOAc/hexanes on silica) gave the title compound (1.8 g, 64%) as a clear oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05646170
Quelldatensatzuspto-grants-1997_07
ORD IDord-bb721834dec940dab7e70644d02dbd7e
Quellennotizuspto-grants-1997_07