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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386312Generated: October 27, 2026

Sodium methanethiolate → Methyl 5-methylthio-2-nitrophenylacetate

https://huagongshe.com/reaction/1386312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
ReactantMethyl 2-(5-fluoro-2-nitrophenyl)acetateHCID 15292019—
SolventDimethyl SulfoxideHCID 679—
ProductMethyl 5-methylthio-2-nitrophenylacetateHCID 2171719081%

Reaction Steps

A solution of methyl 5-fluoro-2-nitrophenylacetate (3 g, 14 mmol), (Synthesis 1993, 51), in DMSO (10 ml) was added to a suspension of sodium thiomethoxide (1.08 g, 15.5 mmol) in anhydrous DMSO (10 ml). The mixture was stirred for 10 minutes at ambient temperature and further sodium thiomethoxide (100 mg, 1.5 mmol) was added. The mixture was stirred for 15 minutes at ambient temperature and was then partitioned between ethyl acetate and water. The organic layer was separated, washed with water, brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with ethyl acetate/petroleum ether (15/85) to give methyl 5-methylthio-2-nitrophenylacetate (2.68 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265411B1
Source datasetuspto-grants-2001_07
ORD IDord-83eb2fe293424a4faf168608662bc061
Source noteuspto-grants-2001_07