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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759427Generated: November 1, 2026

Methyl iodide → HCID 12677424, compound

https://huagongshe.com/reaction/1759427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium MethoxideHCID 10942334—
Reactantalpha-(Methylthio)(m-benzoylphenyl)-acetonitrileHCID 12677423—
SolventMethanolHCID 887—
ProductHCID 12677424HCID 1267742473%

Reaction Steps

433 mg of alpha-(methylthio)(m-benzoylphenyl)-acetonitrile was dissolved in 2 ml of anhydrous methanol. The solution was stirred in an atmosphere of argon under ice cooling. Then, 0.65 ml of a 2.5 M methanol solution of sodium methoxide was added, and then 0.15 ml of methyl iodide was added dropwise. Under ice cooling, the mixture was stirred for 1 hour, and an aqueous solution of ammonium chloride (0.5 g/30 ml) was added. The mixture was extracted with 20 ml of methylene chloride three times. The extract was washed with 10 ml of water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel; methylene chloride) to afford 334 mg (yield 73%) of alpha-(methylthio)-alpha-(m-benzoylphenyl)-propionitrile as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04340740
Source datasetuspto-grants-1982_07
ORD IDord-0a1c2c554b6548bb85cca8924166b5bf
Source noteuspto-grants-1982_07