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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047973Generated: November 1, 2026

Hydrochloric Acid → 5-Methylbenzofuran-7-amine

https://huagongshe.com/reaction/2047973

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 numberUS08592593B2
Source datasetuspto-grants-2013_11
ORD IDord-535bd4a7f507415bb6e753bdcd35242d
Source noteuspto-grants-2013_11