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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660474Generated: October 31, 2026

Methyl iodide → HCID 12917658, compound

https://huagongshe.com/reaction/1660474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 12917657HCID 12917657—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 12917658HCID 1291765893%

Reaction Steps

Methyl α-methylthio[p-[dimethoxy(2-thienyl)methyl]phenyl]acetate (457 mg) was dissolved in 3 ml of anhydrous dimethyl sulfoxide, and 60 mg (65% content) of sodium hydride was added. The mixture was stirred at room temperature for 30 minutes. Then, 0.15 ml of methyl iodide was added, and the mixture was stirred at room temperature for 20 minutes. After adding an aqueous solution of ammonium chloride (0.5 g/30 ml), the mixture was extracted three times with 20 ml of methylene chloride. The extract was washed twice with 10 ml of water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was chromatographed on a Florisil column using benzene as an eluent to give 443 mg of methyl α-methylthio-α-[p-[dimethoxy(2-thienyl)methyl]phenyl]propionate as a colorless oil in a yield of 93%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04308208
Source datasetuspto-grants-1981_12
ORD IDord-4a0abc3f530b476dac02c658deb328f9
Source noteuspto-grants-1981_12