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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391091Generated: October 25, 2026

Methanethiol → 3-(4-Methoxybenzylmercapto)-2-(methylthio)propanoic acid

https://huagongshe.com/reaction/1391091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanethiolHCID 878—
ReactantSodium HydroxideHCID 14798—
Reactant2-Bromo-3-(4-methoxybenzylmercapto)propanoic acidHCID 20385290—
SolventEthanolHCID 702—
Product3-(4-Methoxybenzylmercapto)-2-(methylthio)propanoic acidHCID 54057018—

Reaction Steps

A solution of 2-bromo-3-(4-methoxybenzylmercapto)propanoic acid (15 g.), methylmercaptan (3 g.) and sodium hydroxide (4.6 g.) in 95% ethanol (25 ml.) is refluxed for twelve hours. The sodium bromide is filtered off and the filtrate is concentrated to dryness in vacuo. The residue is dissolved in water, acidified with concentrated hydrochloric acid and extracted with ethyl acetate. The organic layer is dried and concentrated to dryness to yield 3-(4-methoxybenzylmercapto)-2-(methythio)propanoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04140864
Source datasetuspto-grants-1979_02
ORD IDord-ba37de8ceaa246fa9770dd2df872a9d3
Source noteuspto-grants-1979_02