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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582822Generated: October 30, 2026

Ethyl 3-(2-bromoethoxy)-2-methylbenzoate → Ethyl 3-(2-methylsulfonylthioethoxy)-2-methylbenzoate

https://huagongshe.com/reaction/582822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(2-bromoethoxy)-2-methylbenzoateHCID 15376195—
ReactantPotassium thiomethanesulfonateHCID 23696406—
SolventEthanolHCID 702—
ProductEthyl 3-(2-methylsulfonylthioethoxy)-2-methylbenzoateHCID 15376196—

Reaction Steps

2 g (7 mmol) of ethyl 3-(2-bromoethoxy)-2-methylbenzoate and 1.1 g (7.3 mmol) of potassium thiomethanesulfonate are dissolved in 10 ml absolute ethanol. The reaction mixture is refluxed for 20 hours. The solvent is then distilled off and the residue taken up in methylene chloride and washed with water. The organic phase is dried over sodium sulfate and the solvent is removed. The product of value is purified by column chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925767
Source datasetuspto-grants-1999_07
ORD IDord-971a12ba684246ea9e0f633a678e70d6
Source noteuspto-grants-1999_07