HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881364Generated: November 1, 2026
7-Methoxy-2-methyl-4-nitro-1-benzofuran → HCID 11095186, compound
https://huagongshe.com/reaction/1881364
Participants
| Role | Name | HCID | Charge |
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| Reactant | 7-Methoxy-2-methyl-4-nitro-1-benzofuran | HCID 13201901 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11095186 | HCID 11095186 | 58.3% |
Reaction Steps
7-Methoxy-2-methyl-4-nitro-benzofuran (1.24 g, 6.0 mmol) was hydrogenated using Pd/C (10%, dry, 700 mg) and H2 balloon in EtOH (30 mL) at r.t. for 2 h. The reaction mixture was filtered. Purification of the concentrated filtrate by column chromatography (EtOAc:Hexane=2.5:7.5) afforded 7-methoxy-2-methyl-benzofuran-4-ylamine as a brown oil (620 mg, 58%). 7-Methoxy-2-methyl-benzofuran-4-ylamine (620 mg, 3.5 mmol) was dissolved in CH2Cl2 (10 mL). TCDI (thiocarbodiimidazole, 686 mg, 3.9 mmol) was added to the solution and the reaction mixture was stirred at r.t. for 30 min. Silica gel was added to the reaction mixture and the solvent was removed under vacuum. Purification of the silica gel coated crude product by flash column chromatography (EtOAc:Hexane=2:8) afforded the title product as a pale yellow oil (630 mg, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318790B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-d942229692f94ac88491c0027abc6a1a |
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| Source note | uspto-grants-2012_11 |
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