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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485115Generated: October 25, 2026

Ammonia → 2-Amino-2-(4-iodophenyl)acetonitrile

https://huagongshe.com/reaction/1485115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantWaterHCID 962—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant4-IodobenzaldehydeHCID 96657—
SolventMethanolHCID 887—
SolventTitanium isopropoxideHCID 11026—
Product2-Amino-2-(4-iodophenyl)acetonitrileHCID 67151559—

Reaction Steps

To a solution of 4-iodobenzaldehyde (10.4 g) in methanol (36 mL), tetraisopropyl orthotitanate (50.0 mL) and a solution (50 mL) of 8 mol/L ammonia in methanol were added and the mixture was stirred at room temperature for 3.5 hours. Trimethylsilyl cyanide (5.89 mL) was slowly added to the mixture, which was then stirred at the same temperature for 14 hours. Iced water was added to the reaction mixture, which was then filtered through Celite (registered trademark). The filtrate was concentrated under reduced pressure and the resulting residue was extracted with ethyl acetate. The combined organic layers were washed with water and dried over anhydrous magnesium sulfate. The desiccant was removed by filtration and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=99:1-25:75) to give amino(4-iodophenyl)acetonitrile as a pale yellow solid (5.05 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422240B2
Source datasetuspto-grants-2016_08
ORD IDord-e3a69db3aa75466abea85074d02c8e6e
Source noteuspto-grants-2016_08