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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591458Generated: November 4, 2026

Dimethylformamide → Methyl 2-(4-chloro-7-fluoro-6-hydroxy-1-benzothiophen-3-yl)acetate

https://huagongshe.com/reaction/591458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium 2-methyl-2-propanethiolateHCID 5147913—
ReactantMethyl 2-(4-chloro-7-fluoro-6-methoxy-1-benzothiophen-3-yl)acetateHCID 121003826—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductMethyl 2-(4-chloro-7-fluoro-6-hydroxy-1-benzothiophen-3-yl)acetateHCID 12100651784.6%

Reaction Conditions

Temperature160 °C

Reaction Steps

To a mixture of methyl(4-chloro-7-fluoro-6-methoxy-1-benzothiophen-3-yl)acetate (284.8 mg) and DMF (dry) (8.0 mL) was added sodium 2-methyl-2-propanethiolate (443 mg). The mixture was stirred at 160° C. for 45 min. After cooling, the mixture was diluted with water and 1N HCl and extracted with EtOAc. The organic layer was washed successively with water and brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was dissolved in MeOH (6.0 mL). To the solution was added conc. H2SO4 (0.100 mL). The mixture was stirred at 70° C. for 1 h. The mixture was concentrated. The residue was neutralized with saturated aqueous NaHCO3, and the mixture was extracted with EtOAc. The combined organic layer was washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residual solid was washed with toluene and hexane to give the title compound (229.3 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238639B2
Source datasetuspto-grants-2016_01
ORD IDord-3d4b652f45da49e68815334fcb9f8e50
Source noteuspto-grants-2016_01