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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759422Generated: November 1, 2026

Methyl iodide → alpha-(Methylthio)-alpha-(m-phenoxyphenyl)propionitrile

https://huagongshe.com/reaction/1759422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium MethoxideHCID 10942334—
Reactantalpha-(Methylthio)(m-phenoxyphenyl)-acetonitrileHCID 20532029—
SolventMethanolHCID 887—
Productalpha-(Methylthio)-alpha-(m-phenoxyphenyl)propionitrileHCID 5457058982%

Reaction Steps

956 ml of alpha-(methylthio)(m-phenoxyphenyl)-acetonitrile was dissolved in 5 ml of anhydrous methanol, and 1.7 ml of a 2.5 M methanol solution of sodium methoxide was added at room temperature in an atmosphere of argon. The mixture was stirred, and 0.34 ml of methyl iodide was added dropwise. The mixture was further stirred for 1 hour at room temperature. An aqueous solution of ammonium chloride (3 g/20 ml) was added, and the mixture was extracted with 20 ml of ether three times. The extract was washed with 25 ml of water three times, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel; hexane and methylene chloride) to afford 817 mg (yield 82%) of alpha-(methylthio)-alpha-(m-phenoxyphenyl)-propionitrile as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04340740
Source datasetuspto-grants-1982_07
ORD IDord-07bf9d6d959647d4b64ca52a149dc9ec
Source noteuspto-grants-1982_07