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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759421Generated: October 25, 2026

Methyl iodide → alpha-(p-Tolylthio)-alpha-(m-phenoxyphenyl)propionitrile

https://huagongshe.com/reaction/1759421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium MethoxideHCID 10942334—
Reactantalpha-(p-Tolylthio)(m-phenoxyphenyl)-acetonitrileHCID 12945139—
SolventMethanolHCID 887—
Productalpha-(p-Tolylthio)-alpha-(m-phenoxyphenyl)propionitrileHCID 1302316986%

Reaction Steps

1.245 g of alpha-(p-tolylthio)(m-phenoxyphenyl)-acetonitrile was dissolved in 5 ml of anhydrous methanol, and a 2.2 M methanol solution of sodium methoxide was added at room temperature in an atmosphere of argon. The mixture was stirred, and 0.35 ml of methyl iodide was added dropwise. The mixture was further stirred for 30 minutes at room temperature. Then, 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 30 ml of water three times, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The oily residue was purified by column chromatography (silica gel; hexane and methylene chloride) to afford 1.125 g (yield 86%) of alpha-(p-tolylthio)-alpha-(m-phenoxyphenyl)propionitrile as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04340740
Source datasetuspto-grants-1982_07
ORD IDord-41e3db438f8244859a3e784bcced1f33
Source noteuspto-grants-1982_07