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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756953Generated: October 24, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
ReactantTriphenylundecylphosphonium bromideHCID 3085198—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54381600HCID 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-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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05441975
Source datasetuspto-grants-1995_08
ORD IDord-b05c7116fe4842f4b46bea5f2dd6778f
Source noteuspto-grants-1995_08