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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022431Generated: November 2, 2026

Methyl iodide → 2-(4-Bromophenyl)propanenitrile

https://huagongshe.com/reaction/1022431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantBenzeneacetonitrile, 4-bromo-HCID 27914—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Bromophenyl)propanenitrileHCID 1075092753.6%

Reaction Steps

To a stirred solution of 2-(4-bromo phenyl) acetonitrile (20 g, 102.04 mmol) in dry tetrahydrofuran (200 mL) was added sodium bis(trimethylsilyl)amide (18.71 g, 102.04 mmol) at 0° C. under a nitrogen atmosphere. After stirring for 20 minutes at room temperature, methyl iodide (14.48 g, 102 mmol) was added and then stirred for 1 h at room temperature. The reaction mixture was quenched with an aqueous ammonium chloride solution and extracted with ethyl acetate (2×150 mL). The combined organic layers were washed with water (2×100 mL), a saturated aqueous sodium chloride solution (2×25 mL), dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. Flash chromatography (3-4% ethyl acetate/hexanes) afforded 2-(4-bromo-phenyl)-propionitrile as a light yellow liquid (11.5 g, 53.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722661B2
Source datasetuspto-grants-2014_05
ORD IDord-6424866992f344d2bdc5efe5cec9a5e0
Source noteuspto-grants-2014_05