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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489599Generated: October 30, 2026

Methyl iodide → 3-(Cyanomethyl)benzonitrile

https://huagongshe.com/reaction/489599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium CyanideHCID 8929—
ReactantBenzonitrile, 3-(bromomethyl)-HCID 97249—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-(Cyanomethyl)benzonitrileHCID 519280102%

Reaction Steps

To a solution of 9.8 g (200 mmole) of sodium cyanide and 1.61 g (5 mmole) of tetrabutylammonium bromide in 50 ml of water was added a solution of 19.61 g (100 mmole) of α-bromo-m-tolunitrile in 150 ml of dichloromethane. The mixture was stirred at room temperature for 24 hours. To this mixture was added 6.2 ml (100 mmole) of iodomethane. The mixture was stirred at room temperature for 3 hours. The layers were separated and the organic layer was dried over magnesium sulfate and was filtered. The filtrate was evaporated and the residue was triturated with petroleum ether and the insoluble material was collected to give 14.5 g of a white solid, mp-66-9° C.; 100% yield: 1H-NMR (300 MHz, CDCl3) δ (TMS) 3.80-3.90(s, 2H), 7.49-7.72(m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06977263B2
Source datasetuspto-grants-2005_12
ORD IDord-ede4bd1a89314a6ea8808ca8b2383d24
Source noteuspto-grants-2005_12