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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841310Generated: November 1, 2026

Water → 2-(2-Fluoro-4-iodophenyl)acetonitrile

https://huagongshe.com/reaction/841310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CyanideHCID 8929—
Reactant1-(Bromomethyl)-2-fluoro-4-iodobenzeneHCID 22240406—
SolventEthanolHCID 702—
Product2-(2-Fluoro-4-iodophenyl)acetonitrileHCID 2224053296.4%

Reaction Steps

A solution of 2-fluoro-4-iodo-benzyl bromide (Intermediate 1, 2.56 g, 8.15 mmol) in ethanol (55 mL and water (10 mL) was treated with sodium cyanide (2.15 g, 43.86 mmol) and refluxed for 0.5 h. The volatiles were distilled off in vacuo and the residue was diluted with water and extracted with diethyl ether (×2). The combined organic extract was washed with water (×1) and brine (×1), dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford the title compound as a pale yellow solid (2.05 g, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369225B1
Source datasetuspto-grants-2002_04
ORD IDord-b478eddcb88d418e9d3613e45b4226d0
Source noteuspto-grants-2002_04