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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178816Generated: November 2, 2026

Ethyl(5-methoxy-1-benzofuran-3-yl)acetate → 2-(5-Methoxy-1-benzofuran-3-yl)ethanol

https://huagongshe.com/reaction/1178816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl(5-methoxy-1-benzofuran-3-yl)acetateHCID 15618718—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product2-(5-Methoxy-1-benzofuran-3-yl)ethanolHCID 14982873—

Reaction Steps

To a stirred suspension of LiAlH4 (200 mg, excess) in THF at 0° C., ethyl(5-methoxy-1-benzofuran-3-yl)acetate (1.17 g, 5 mmol) in THF (20 ml) was added slowly. After the addition, reaction mixture was stirred at room temperature for 1 hr and quenched with saturated NH4Cl solution. The product was extracted with chloroform and washed well with water. It was dried over anhydrous MgSO4, filtered and concentrated. The product, 2-(5-methoxy-1-benzofuran-3-yl)ethanol, was obtained as a white oil and was pure enough to be taken to the next step without purification, yielding a yellow oil. Yield: 900 mg (93%); (M+H): 193.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276603B2
Source datasetuspto-grants-2007_10
ORD IDord-6a7214f3afad4e2f86a942ee10598db4
Source noteuspto-grants-2007_10