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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76874Generated: October 25, 2026

4-Iodo-1-tritylimidazole → 3-Fluoro-4-(5-iodo-imidazol-1-ylmethyl)benzonitrile

https://huagongshe.com/reaction/76874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Iodo-1-tritylimidazoleHCID 618252—
Reactant4-(Bromomethyl)-3-fluorobenzonitrileHCID 2783149—
SolventAcetonitrileHCID 6342—
Product3-Fluoro-4-(5-iodo-imidazol-1-ylmethyl)benzonitrileHCID 58827215—

Reaction Steps

A mixture of 4-iodo-1-trityl-1H-imidazole (17.1 g, 39.2 mmol) and 4-bromomethyl-3-fluorobenzonitrile (9.65 g, 45.08 mmol) in 150 mL of dry acetonitrile is stirred at room temperature for 7 days. After concentration, the residue is mixed with methanol, and heated to reflux for 1.5 h. The solvent is subsequently removed and the residue is treated with 1M HCl (300 mL). The resulting suspension is filtered and the washed with HCl (1 M). The combined solution is adjusted to PH 9-10 by saturated NaHCO3 solution. The resulting precipitation is collected by filtration, dried in vacuum oven. MS (ESI) m/z (M+H) 328.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835646B2
Source datasetuspto-grants-2014_09
ORD IDord-00356ce0b93c4b9eb25ec3d05af4d485
Source noteuspto-grants-2014_09