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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706018Generated: October 31, 2026

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

https://huagongshe.com/reaction/1706018

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-(methylthio)propanoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04206121
Source datasetuspto-grants-1980_06
ORD IDord-6563aa555e044da7b772ab5dd25bfc52
Source noteuspto-grants-1980_06