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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444447Generated: October 25, 2026

Methyl iodide → 2-(2-Bromophenyl)propanenitrile

https://huagongshe.com/reaction/1444447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromobenzyl cyanideHCID 29625—
SolventDimethylformamideHCID 6228—
Product2-(2-Bromophenyl)propanenitrileHCID 10608494—

Reaction Steps

18.9 g (96.41 mmol) of (2-bromophenyl)-acetonitrile and 31.41 g (221.74 mmol) of methyl iodide are dissolved in 150 ml of N,N-dimethylformamide. At 0° C., 8.87 g (221.74 mmol) of sodium hydride (as 60% suspension in oil) is added in portions, and the batch is stirred overnight at room temperature. The reaction mixture is poured into ice water and worked up as usual. Since the compound that is isolated after chromatography (20.9 g) still contains 2-(2-bromophenyl)-propionitrile in addition to the desired product, the entire amount is reacted another time with the same amounts of reagent. This reaction also yields only material that still contains mono-methyl compound. After another alkylation with 15 g of methyl iodide and 4.45 g of sodium hydride in 150 ml of N,N-dimethylformamide, 18.57 g of the desired compound is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662821B2
Source datasetuspto-grants-2010_02
ORD IDord-6b556fc2b3be47679adf3dcdf4f10765
Source noteuspto-grants-2010_02