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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258515Generated: November 2, 2026

Hydrochloric Acid → 7-Chloro-2-(2-hydroxymethylbenzofuran-5-yl)quinoline

https://huagongshe.com/reaction/2258515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant7-Chloro-2-(2-methoxycarbonylbenzofuran-5-yl)quinolineHCID 22922182—
SolventTetrahydrofuranHCID 8028—
Product7-Chloro-2-(2-hydroxymethylbenzofuran-5-yl)quinolineHCID 22922214—

Reaction Steps

To a mixture of 7-chloro-2-(2-methoxycarbonylbenzofuran-5-yl)quinoline (0.92 g) in tetrahydrofuran (10 ml), lithium aluminum hydride (76.7 mg) was added dropwise under ice cooling. After being stirred for 2 hours, the resulting mixture was poured into a mixture of ice and diluted aqueous hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to column chromatography on silica gel and eluted with a mixture of ethyl acetate and toluene. The fractions containing object compound were combined, concentrated under reduced pressure, and recrystallized from toluene to give 7-chloro-2-(2-hydroxymethylbenzofuran-5-yl)quinoline (0.58

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05661159
Source datasetuspto-grants-1997_08
ORD IDord-988932bb048d42f0970fe16d23392df4
Source noteuspto-grants-1997_08