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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602429Generated: November 2, 2026

2,3-Dihydro-1-benzofuran-4-carboxylic acid → (2,3-Dihydro-1-benzofuran-4-yl)methanol

https://huagongshe.com/reaction/1602429

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydro-1-benzofuran-4-carboxylic acidHCID 18787444—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(2,3-Dihydro-1-benzofuran-4-yl)methanolHCID 18787415—

Reaction Steps

A solution of 2,3-dihydrobenzofuran-4-carboxylic acid (10 g, 61 mmol) in THF (100 mL) was stirred as LAH (4.64 g, 122 mmol) was slowly added. The mixture was heated to reflux for 30 min. The mixture was cooled and quenched cautiously with ethyl acetate and then with 1N HCl (150 mL). The mixture was then made acidic with 12N HCl until all the inorganic precipitate dissolved. The organic layer was separated, and the inorganic layer was extracted twice with ethyl acetate. The organic layers were combined, washed twice with brine, and then concentrated in vacuo. This oil was Kugelrohr distilled to a clear oil that crystallized upon cooling (8.53 g, 87.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981571
Source datasetuspto-grants-1999_11
ORD IDord-7a4e7ce673544ab4881d887e447fae70
Source noteuspto-grants-1999_11