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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591467Generated: October 31, 2026

Methanol → (7-Chloro-6-((2,4-dichlorobenzyl)oxy)-1-benzofuran-3-yl)acetic acid

https://huagongshe.com/reaction/591467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl(7-chloro-6-((2,4-dichlorobenzyl)oxy)-1-benzofuran-3-yl)acetateHCID 118667011—
SolventTetrahydrofuranHCID 8028—
Product(7-Chloro-6-((2,4-dichlorobenzyl)oxy)-1-benzofuran-3-yl)acetic acidHCID 8976819587.1%

Reaction Steps

To a mixture of methyl(7-chloro-6-((2,4-dichlorobenzyl)oxy)-1-benzofuran-3-yl)acetate (218.9 mg), MeOH (2.0 mL) and THF (dry) (2.0 mL) was added 1N NaOH (1.643 mL) at room temperature. The mixture was stirred at room temperature for 2 h. The residue was concentrated. The residue was neutralized with 1N HCl, and the mixture was extracted with EtOAc. The combined organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The precipitate was collected by filtration, and crystallized from EtOH-hexane to give the title compound (184 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238639B2
Source datasetuspto-grants-2016_01
ORD IDord-84c93ce63f6846dcb6dc17b4e70d92c5
Source noteuspto-grants-2016_01