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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935761Generated: November 1, 2026

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

https://huagongshe.com/reaction/1935761

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 numberUS06387892B1
Source datasetuspto-grants-2002_05
ORD IDord-ab0d2d2076f344dab4c987b55ac9349d
Source noteuspto-grants-2002_05