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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861314Generated: November 2, 2026

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

https://huagongshe.com/reaction/1861314

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 numberUS06531599B2
Source datasetuspto-grants-2003_03
ORD IDord-e0798264c48046b5a9ee5ba19d7f6810
Source noteuspto-grants-2003_03