Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733633Generated: November 1, 2026

Methyl iodide → Methyl alpha-methylthio-alpha-(m-(alpha,alpha-dimethoxybenzyl)phenyl)propionate

https://huagongshe.com/reaction/1733633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl alpha-methylthio-[m-(alpha,alpha-dimethoxybenzyl)phenyl]acetateHCID 20556707—
SolventDimethyl SulfoxideHCID 679—
ProductMethyl alpha-methylthio-alpha-(m-(alpha,alpha-dimethoxybenzyl)phenyl)propionateHCID 1281945284%

Reaction Steps

Methyl α-methylthio-[m-(α,α-dimethoxybenzyl)phenyl]acetate (444 mg) was dissolved in 4 ml of dimethyl sulfoxide, and 55 mg of sodium hydride (65% content) was added. The mixture was stirred at room temperature for 20 minutes. Methyl iodide (0.20 ml) was added dropwise over the course of 3 minutes, and the mixture was further stirred at room temperature for 30 minutes. An aqueous solution of ammonium chloride (200 mg/30 ml) was added, and the mixture was extracted three times with 20 ml of diethyl ether. The organic layer was washed three times with 10 ml of water, dried over anhydrous sodium sulfate, and the residue was chromatographed on a column of Florisil using benzene and methylene chloride as eluents to afford 386 mg of methyl α-methylthio-α-[m-(α,α-dimethoxybenzyl)phenyl]propionate as an oil in a yield of 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242519
Source datasetuspto-grants-1980_12
ORD IDord-ddaeef7462b14a88814c036b0ae68f00
Source noteuspto-grants-1980_12