HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68136Generated: October 28, 2026
Hydrochloric Acid → 5-Methylbenzofuran-7-amine
https://huagongshe.com/reaction/68136
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 58492450 | HCID 58492450 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Methylbenzofuran-7-amine | HCID 55284827 | 2,980.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE045108E1 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-16b0765578604f18b887cc78dc92088b |
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| Source note | uspto-grants-2014_09 |
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