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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187600Generated: October 30, 2026

Ethanol → Methyl 2-[(5-benzofuranyloxy)methyl]benzoate

https://huagongshe.com/reaction/2187600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-(bromomethyl)benzoateHCID 2734813—
CatalystHCID 178418390HCID 178418390—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 22397060HCID 2239706017%
ProductMethyl 2-[(5-benzofuranyloxy)methyl]benzoateHCID 2239706927%

Reaction Conditions

Temperature100 °C

Reaction Steps

5-(Benzyloxy)benzofuran (1.02 g, 4.55 mmol) obtained in Preparation Example 2-4, Step 2 was dissolved in a mixed solvent of ethanol (5 ml) and ethyl acetate (5 ml) and 5% palladium carbon (500 mg) was added, which was followed by hydrogenation at room temperature under normal pressure. After 2 hr, the reaction mixture was passed through celite and the filtrate was concentrated under reduced pressure. The residue was dissolved in dimethylformamide (20 ml) and methyl α-bromo-o-toluate (1.042 g, 4.55 mmol) and potassium carbonate (1.26 g, 9.10 mmol) were added. The mixture was heated at 100° C. for 1.25 hr and cooled to room temperature. The reaction mixture was diluted with water and ethyl acetate to separate the layers. The organic layer was washed with saturated aqueous sodium hydrogencarbonate solution and saturated brine, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1) to give methyl 2-[(5-benzofuranyloxy)methyl]benzoate (352 mg, 27%, white crystals) and methyl 2-[(2,3-dihydrobenzofuran-5-yloxy)methyl]benzoate (220 mg, 17%, pale-yellow oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410561B1
Source datasetuspto-grants-2002_06
ORD IDord-cdc4ab544a4f4b8a956ed67fb7000bc3
Source noteuspto-grants-2002_06