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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591472Generated: October 30, 2026

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

https://huagongshe.com/reaction/591472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl(6-((2,4-dichlorobenzyl)oxy)-4,7-dimethyl-1-benzofuran-3-yl)acetateHCID 71721635—
SolventTetrahydrofuranHCID 8028—
Product(6-((2,4-Dichlorobenzyl)oxy)-4,7-dimethyl-1-benzofuran-3-yl)acetic acidHCID 8976806183.2%

Reaction Steps

To a mixture of methyl(6-((2,4-dichlorobenzyl)oxy)-4,7-dimethyl-1-benzofuran-3-yl)acetate (147 mg), MeOH (2.0 mL) and THF (dry) (2.0 mL) was added 1N NaOH (1.12 mL) at room temperature. The mixture was stirred at room temperature for 2 h, and then concentrated in vacuo. The residue was neutralized with 1N HCl, and the mixture was extracted with EtOAc. The organic layer was washed with brine and, dried over MgSO4, and concentrated in vacuo. The precipitate was collected by filtration, and crystallized from EtOAc-hexane to give the title compound (118 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238639B2
Source datasetuspto-grants-2016_01
ORD IDord-7ca562ccaeaa456b87eb5a4a0031fedf
Source noteuspto-grants-2016_01