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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874028Generated: October 31, 2026

Hydrochloric Acid → 5-Methylbenzofuran-7-amine

https://huagongshe.com/reaction/1874028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 58492450HCID 58492450—
SolventTetrahydrofuranHCID 8028—
Product5-Methylbenzofuran-7-amineHCID 552848272,980.1%

Reaction Steps

Benzhydrylidene(5-methylbenzofuran-7-yl)amine (17.9 g, 0.57 mmol) was dissolved in THF (150 ml). 5N Hydrochloric acid (50 ml) was added thereto, followed by stirring at room temperature for 2 hours. A 5N aqueous sodium hydroxide solution (40 ml) was added to the reaction mixture, followed by extraction using ethyl acetate. The extract was sequentially washed with an aqueous saturated sodium hydrogen solution and an aqueous saturated sodium chloride solution. The organic layer was dried over magnesium sulfate and concentrated to dryness under reduced pressure. The residue was purified using silica gel column chromatography (n-hexane:ethyl acetate=50:1→10:1). The purified product was concentrated to dryness under reduced pressure, giving a dark brown oily substance of 5-methylbenzofuran-7-ylamine (2.5 g, yield: 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304546B2
Source datasetuspto-grants-2012_11
ORD IDord-0558c135951f4b83855bf068bb25c692
Source noteuspto-grants-2012_11