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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1756953Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1756953

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 JL, Miller CA, and McLean EW, 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
PatentnummerUS05441975
Quelldatensatzuspto-grants-1995_08
ORD IDord-b05c7116fe4842f4b46bea5f2dd6778f
Quellennotizuspto-grants-1995_08