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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591561Generated: October 29, 2026

Methanesulfonic Acid → Methyl(4-fluoro-6-methoxy-1-benzothiophen-3-yl)acetate

https://huagongshe.com/reaction/591561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantMethyl 4-((3-fluoro-5-methoxyphenyl)sulfanyl)-3-oxobutanoateHCID 89768091—
SolventWaterHCID 962—
ProductMethyl(4-fluoro-6-methoxy-1-benzothiophen-3-yl)acetateHCID 12547428733.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

MsOH (13.68 mL) was added dropwise to methyl 4-((3-fluoro-5-methoxyphenyl)sulfanyl)-3-oxobutanoate (2.87 g) at 0° C. The mixture was stirred at 0° C. for 30 min. The mixture was poured into iced water and extracted with EtOAc. The organic layer was separated, washed successively with water, saturated aqueous NaHCO3 and brine, dried over MgSO4 and concentrated in vacuo. The residue was purified by silica gel column chromatography (EtOAc/hexane) to give the title compound (900 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238639B2
Source datasetuspto-grants-2016_01
ORD IDord-64e057bd6688444b9a8cb568ede9e004
Source noteuspto-grants-2016_01