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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186739Generated: October 29, 2026

Potassium Carbonate → Methyl 3-(2-hydroxyethyl)-2,3-dihydrobenzofuran-7-yloxyacetate

https://huagongshe.com/reaction/2186739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl bromoacetateHCID 60984—
Reactant7-Hydroxy-3-(2-hydroxyethyl)benzofuranHCID 11159639—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(2-hydroxyethyl)-2,3-dihydrobenzofuran-7-yloxyacetateHCID 2244896174%

Reaction Steps

7-hydroxy-3-(2-hydroxyethyl)benzofuran (7.01 g) was dissolved in dimethylformamide (100 ml), and potassium carbonate (5.76 g) and methyl bromoacetate (4.74 ml) were added to the resultant solution, and the mixture was stirred at room temperature for 21 hours. The reaction solution was filtered with Celite, and the filtrate was concentrated. Ethyl acetate (300 ml) was added to the residue, and then the mixture was washed with water and saturated brine, and dried over sodium sulfate. After sodium sulfate was filtered off, the filtrate was concentrated, and the residue was dissolved in methanol (100 ml). 5% Pd/C (1.0 g), and acetic acid (5 ml) were added to the resultant solution, and the mixture was stirred at room temperature for 23 hours under a hydrogen atmosphere. The reaction solution was filtered with Celite, and the filtrate was concentrated. Ethyl acetate (300 ml) was added to the residue, and the mixture was washed with water and saturated brine, and dried over sodium sulfate. After sodium sulfate was filtered off, the filtrate was concentrated, and the residue was purified by flash column chromatography using silica gel (elution solvent:hexane/ethyl acetate=1/2) to obtain the object compound (7.80 g, yield 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407096B1
Source datasetuspto-grants-2002_06
ORD IDord-b102efe757bc4980bf2f1ff8c96ff3ea
Source noteuspto-grants-2002_06