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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104962Generated: October 31, 2026

4-phenyl-1-(triphenylmethyl)-1H-imidazole → (5-ethoxy-2-fluoro-3-isopropoxyphenyl)(4-phenyl-1-trityl-1H-imidazol-2-yl)methanol

https://huagongshe.com/reaction/2104962

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-phenyl-1-(triphenylmethyl)-1H-imidazoleHCID 10221769—
Reactant5-Ethoxy-2-fluoro-3-isopropoxybenzaldehydeHCID 86247209—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(5-ethoxy-2-fluoro-3-isopropoxyphenyl)(4-phenyl-1-trityl-1H-imidazol-2-yl)methanolHCID 6881319675.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of Intermediate 8.1 (200 mg, 0.517 mmol) in 3 mL THF at 0° C., was added BuLi (1.4 M in THF, 0.406 mL, 0.569 mmol). The mixture was stirred at 0° C. for 25 min, then a solution of Intermediate 7.2 (117 mg, 0.517 mmol) in 1 mL THF was added dropwise. The mixture was stirred at 0° C. for 30 min, then was quenched with sat. NH4Cl. The mixture was diluted with EtOAc, washed with H2O and brine, dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography (0 to 40% EtOAc/hexanes gradient) to afford 240 mg of Intermediate 25.1 as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576098B2
Source datasetuspto-grants-2009_08
ORD IDord-82c678c85dfc489099ebd5eff43e4600
Source noteuspto-grants-2009_08