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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591465Generated: October 27, 2026

Methanol → Methyl(7-chloro-6-hydroxy-1-benzofuran-3-yl)acetate

https://huagongshe.com/reaction/591465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant(7-Chloro-6-hydroxy-1-benzofuran-3-yl)acetic acidHCID 89767735—
ProductMethyl(7-chloro-6-hydroxy-1-benzofuran-3-yl)acetateHCID 119086644—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of (7-chloro-6-hydroxy-1-benzofuran-3-yl)acetic acid (1.65 g) and MeOH (40 mL) was added conc. H2SO4 (0.078 mL). The mixture was stirred at 60° C. for 3 h. The mixture was concentrated in vacuo. 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 residue was dissolved in toluene and hexane. The insoluble material was filtered and washed with toluene and hexane. The filtrate was purified by silica gel column chromatography (EtOAc/hexane) to give the title compound (1.49 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238639B2
Source datasetuspto-grants-2016_01
ORD IDord-7bfd9c1e8294487f9bd6561e1e76daf0
Source noteuspto-grants-2016_01