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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938715Generated: October 27, 2026

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

https://huagongshe.com/reaction/1938715

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 numberUS05693657
Source datasetuspto-grants-1997_12
ORD IDord-912f9f280b394cc4987dcf4208bed857
Source noteuspto-grants-1997_12