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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591457Generated: November 1, 2026

Methanesulfonic Acid → Methyl 2-(4-chloro-7-fluoro-6-methoxy-1-benzothiophen-3-yl)acetate

https://huagongshe.com/reaction/591457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantMethyl 4-((5-chloro-2-fluoro-3-methoxyphenyl)sulfanyl)-3-oxobutanoateHCID 89767787—
ProductMethyl 2-(4-chloro-7-fluoro-6-methoxy-1-benzothiophen-3-yl)acetateHCID 12100382689.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

MsOH (4.0 mL) was added to methyl 4-((5-chloro-2-fluoro-3-methoxyphenyl)sulfanyl)-3-oxobutanoate (400 mg) at 0° C. After stirring at 0° C. for 20 min, the mixture was warmed to room temperature and stirred for 2 h. The mixture was poured into ice water at 0° C. and extracted with EtOAc. The organic layer was separated, washed successively with 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 (338 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238639B2
Source datasetuspto-grants-2016_01
ORD IDord-84b1bfb551484127aab4c47e31d72b3b
Source noteuspto-grants-2016_01