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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733611Generated: November 2, 2026

Triethylamine → 1,1-Bis(methylthio)-2-chloro-2-(p-isobutylphenyl) ethylene

https://huagongshe.com/reaction/1733611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant1-Methylsulfinyl-1-methylthio-2-(p-isobutylphenyl)ethyleneHCID 54562612—
SolventChloroformHCID 6212—
Product1,1-Bis(methylthio)-2-chloro-2-(p-isobutylphenyl) ethyleneHCID 1281946284%

Reaction Steps

1-Methylsulfinyl-1-methylthio-2-(p-isobutylphenyl)ethylene (701 mg) was dissolved in 2 ml of chloroform, and 0.50 ml of triethylamine was added. With stirring under ice cooling, 5 ml of a chloroform solution of 380 mg of thionyl chloride was added over the course of 10 minutes. The mixture was further stirred for 30 minutes under ice cooling, and chloroform was added in an amount sufficient to adjust the total amount of the mixture to 30 ml. The mixture was then washed twice with 10 ml of water. The organic layer was dried over anhydrous sodium sulfate, concentrated under reduced pressure, and chromatographed on a Florisil (chromatographic magnesium silicate) column using benzene as an eluent to afford 628 mg of 1,1-bis (methylthio)-2-chloro-2-(p-isobutylphenyl) ethylene as a colorless oil in a yield of 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242519
Source datasetuspto-grants-1980_12
ORD IDord-496ad6acbaac4d3d85362910e704e42a
Source noteuspto-grants-1980_12