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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380502Generated: October 27, 2026

1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde → 4-(1-Dodecenyl)-1-(triphenylmethyl)imidazole

https://huagongshe.com/reaction/2380502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
ReactantTriphenylundecylphosphonium bromideHCID 3085198—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-(1-Dodecenyl)-1-(triphenylmethyl)imidazoleHCID 5438160064%

Reaction Steps

A solution of n-BuLi (4.1 mL, 6.5 mmol, 1.6M in hexanes) was added dropwise to a suspension of n-undecyl-triphenylphosphonium bromide (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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05366987
Source datasetuspto-grants-1994_11
ORD IDord-113106ade4ab4fdc9df75ad3db22414a
Source noteuspto-grants-1994_11