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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1444447Erstellt: 24. Oktober 2026

Methyl iodide → 2-(2-Bromophenyl)propanenitrile

https://huagongshe.com/de/reaction/1444447

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
Edukt2-Bromobenzyl cyanideHCID 29625—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(2-Bromophenyl)propanenitrileHCID 10608494—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07662821B2
Quelldatensatzuspto-grants-2010_02
ORD IDord-6b556fc2b3be47679adf3dcdf4f10765
Quellennotizuspto-grants-2010_02