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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767999Generated: October 27, 2026

Ethyl(5-chloro-1-benzofuran-3-yl)acetate → 2-(5-Chloro-1-benzofuran-3-yl)ethanol

https://huagongshe.com/reaction/1767999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl(5-chloro-1-benzofuran-3-yl)acetateHCID 12936153—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product2-(5-Chloro-1-benzofuran-3-yl)ethanolHCID 23614438—

Reaction Steps

To a stirred suspension of LiAlH4 (200 mg, excess) in THF at 0° C., ethyl(5-chloro-1-benzofuran-3-yl)acetate (1.19 g, 50 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-chloro-1-benzofuran-3-yl)ethanol, was obtained as a white oil pure enough to be taken to the next step without purification. Yield: 850 mg (86%); 197 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235569B2
Source datasetuspto-grants-2007_06
ORD IDord-56ce5de6d94443a6b9939efe9a4d9c95
Source noteuspto-grants-2007_06