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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178792Generated: October 25, 2026

Ethyl 2-(benzofuran-3-yl)acetate → 2-(Benzofuran-3-yl)ethanol

https://huagongshe.com/reaction/1178792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(benzofuran-3-yl)acetateHCID 7537531—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product2-(Benzofuran-3-yl)ethanolHCID 10953836—

Reaction Steps

To a stirred suspension of LiAlH4 (200 mg, excess) in THF at 0° C., ethyl(-1-benzofuran-3-yl)acetate (1.02 g, 5 mmol) in THF (20 mL) was added slowly. After the addition, the 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-(1-benzofuran-3-yl)ethanol obtained as a white oil was pure enough to be taken to next step without further purification. Yield: 800 mg (98%); (M+H): 163.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276603B2
Source datasetuspto-grants-2007_10
ORD IDord-94884fb59d264a6bb5f25fae8ba84b0b
Source noteuspto-grants-2007_10