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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602443Generated: November 2, 2026

Methyl benzofuran-7-carboxylate → Benzofuran-7-ylmethanol

https://huagongshe.com/reaction/1602443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl benzofuran-7-carboxylateHCID 14229730—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
ProductBenzofuran-7-ylmethanolHCID 1878742291%

Reaction Steps

A solution of methyl benzofuran-7-carboxylate (5.34 g, 30 mmol) was added to a suspension of LAH (2.31 g, 61 mmol) in THF and then heated to reflux for 30 min. The reaction was quenched with ethyl acetate and water. The mixture was made acidic with 12N HCl until all the precipitate dissolved. The ethyl acetate layer was separated, washed with water, dried with brine, and concentrated in vacuo to give a yellow oil (4.03 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981571
Source datasetuspto-grants-1999_11
ORD IDord-c1ff4e68e9c840dabb6e9364425ef5d7
Source noteuspto-grants-1999_11