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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660438Generated: October 26, 2026

Methyl iodide → Methyl alpha-methylthio-alpha-(m-phenoxyphenyl)propionate

https://huagongshe.com/reaction/1660438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl alpha-methylthio(m-phenoxyphenyl)acetateHCID 20556696—
SolventDimethylformamideHCID 6228—
ProductMethyl alpha-methylthio-alpha-(m-phenoxyphenyl)propionateHCID 1291766294%

Reaction Steps

Methyl α-methylthio(m-phenoxyphenyl)acetate (1.963 g) was dissolved in anhydrous dimethylformamide, and under ice cooling, 280 mg (65% content) of sodium hydride was added. The mixture was stirred for 10 minutes. Then, 0.60 ml of methyl iodide was added, and the mixture was stirred under ice cooling for 5 minutes and then at room temperature for 30 minutes. After adding an aqueous solution of ammonium chloride (500 mg/40 ml), the reaction 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 concentrated under reduced pressure. The residue was chromatographed on a silica gel column using hexane and benzene as eluents to afford 1.930 g of methyl α-methylthio-α-(m-phenoxyphenyl)propionate as an oil in a yield of 94%. Distillation of this substance gave a fraction boiling at 147°-149° C./0.08 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04308208
Source datasetuspto-grants-1981_12
ORD IDord-04d86e6f77bf40958888b97d2ec8c744
Source noteuspto-grants-1981_12