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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067667Generated: October 31, 2026

1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde → HCID 178440796, compound

https://huagongshe.com/reaction/1067667

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
Reactant2-Methylpropan-2-olateHCID 4574913—
ReactantPotassiumHCID 5462222—
Reactant3-Phenylpropyl triphenylphosphonium bromideHCID 10928647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178440796HCID 178440796—

Reaction Steps

10 mmol of 3-phenylpropyltriphenylphosphonium bromide, 10 mmol of (1-triphenylmethyl-1H-imidazol-4-yl)methanal (J. L. Kelley, C. A. Miller, E. W. Mc Lean, J. Med. Chem. 1977, 20, 721) and 12 mmol of potassium of t-butanolate are stirred for 24 hours in 50 ml THF. The solvent is evaporated off under reduced pressure, hydrolysed with water and extracted using chloroform. The concentrated organic extract is heated from reflux in 30 ml 2N HCl and 30 ml of acetone for 1 hour. The solvent is evaporated off under reduced pressure and triphenylmethanol is extracted using diethyl ether. The aqueous phase is alkalized using ammonia and the crude product is extracted using diethyl ether. The aqueous phase is alkalized using diethyl ether and crystallized as hydrogen maleate from diethyl ether and ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248765B1
Source datasetuspto-grants-2001_06
ORD IDord-a4c6ae19dac64578b2008e550852aea2
Source noteuspto-grants-2001_06