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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594887Generated: October 27, 2026

4-Iodo-1-tritylimidazole → (4-Cyano-3-fluorophenyl)[1-(triphenylmethyl)imidazol-4-yl]methanol

https://huagongshe.com/reaction/1594887

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Iodo-1-tritylimidazoleHCID 618252—
Reactant2-Fluoro-4-formylbenzonitrileHCID 11217339—
ReactantHCID 178418443HCID 178418443—
SolventDichloromethaneHCID 6344—
Product(4-Cyano-3-fluorophenyl)[1-(triphenylmethyl)imidazol-4-yl]methanolHCID 11134299—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4-iodo-1-trityl-1H-imidazole (5.00 g, 11.5 mmol) in anhydrous CH2Cl2 (30 mL) was added a 3.0M solution of ethylmagnesium bromide (6.58 mL, 19.7 mmol) with stirring under Ar. After 3 h, the reaction mixture was cooled to −78° C. and a solution of 2-fluoro-4-formyl-benzonitrile (as described in Step A above) (1.70 g, 11.5 mmol) dissolved in CH2Cl2 (20 mL) was added dropwise. The reaction was allowed to warm to RT over 2 h, quenched with saturated NH4Cl solution, diluted with satd. NaHCO3 solution to pH=8.5, and extracted with CH2Cl2 (3×). The combined organic layers were dried (MgSO4), concentrated and purified using SiO2 chromatography (0-1% MeOH/CH2Cl2) to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06284755B1
Source datasetuspto-grants-2001_09
ORD IDord-d78255479d3345df96a0146c8a8c0251
Source noteuspto-grants-2001_09