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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591431Generated: November 1, 2026

Methanol → Methyl(4,7-dichloro-6-hydroxy-1-benzothiophen-3-yl)acetate

https://huagongshe.com/reaction/591431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant(4,7-Dichloro-6-hydroxy-1-benzothiophen-3-yl)acetic acidHCID 89768012—
ProductMethyl(4,7-dichloro-6-hydroxy-1-benzothiophen-3-yl)acetateHCID 121006406—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of methyl(4,7-dichloro-6-methoxy-1-benzothiophen-3-yl)acetate (300.9 mg), DMF (dry) (9.0 mL) and sodium 2-methyl-2-propanethiolate (442 mg) was stirred at 160° C. for 20 min. The mixture was quenched with water and 1N HCl and extracted with EtOAc. The organic layer was washed successively with water and brine, dried over MgSO4, and concentrated in vacuo to give (4,7-dichloro-6-hydroxy-1-benzothiophen-3-yl)acetic acid (327 mg) as a crude mixture. A crude mixture of (4,7-dichloro-6-hydroxy-1-benzothiophen-3-yl)acetic acid (369 mg) was dissolved in MeOH (10 mL). To the solution was added conc. H2SO4 (0.100 mL). The mixture was stirred at 80° C. for 40 min. The mixture was concentrated. The residue was neutralized with saturated aqueous NaHCO3 and extracted with EtOAc. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The solid was washed with hexane to give the title compound (345 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238639B2
Source datasetuspto-grants-2016_01
ORD IDord-c01fd56289e04958b926bf99badd8608
Source noteuspto-grants-2016_01