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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107527Generated: October 31, 2026

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

https://huagongshe.com/reaction/1107527

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 12 N 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 numberUS06060506
Source datasetuspto-grants-2000_05
ORD IDord-5f756922f6444bb991b86dd0d2145820
Source noteuspto-grants-2000_05