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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877935Generated: October 26, 2026

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

https://huagongshe.com/reaction/1877935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Iodo-1-tritylimidazoleHCID 618252—
Reactant4-(Bromomethyl)-3-fluorobenzonitrileHCID 2783149—
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 actetonitrile 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 (1M). 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 numberUS08314097B2
Source datasetuspto-grants-2012_11
ORD IDord-d109e669c20d461f85ddf495682f00df
Source noteuspto-grants-2012_11