HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354054Generated: November 1, 2026
Stannous chloride dihydrate → Methyl 7-aminobenzofuran-4-carboxylate
https://huagongshe.com/reaction/354054
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | Methyl 7-nitrobenzofuran-4-carboxylate | HCID 20738655 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 7-aminobenzofuran-4-carboxylate | HCID 14939320 | 88.1% |
Reaction Steps
Tin (II) chloride dihydrate (15.0 g, 66.5 mmol) was added to a suspension of 7-nitro-benzofuran-4-carboxylic acid methyl ester (4.82 g, 21.8 mmol) in ethyl acetate (80 mL) and ethanol (80 mL). The reaction mixture was stirred at room temperature for four days then partitioned between ethyl acetate and saturated aqueous solution of potassium carbonate. The organic extract was washed with brine, dried (anhydrous sodium sulfate) and concentrated under reduced pressure. The residue was purified by flash column chromatography over silica gel eluting with 30% ethyl acetate in hexane give 7-amino-benzofuran-4-carboxylic acid methyl ester (3.67 g, 88%). 1H NMR (CDCl3) δ: 3.92 (s, 3H), 6.60 (d, 1H, J=8.2 Hz), 7.34 (d, 1H, J=2.1 Hz), 7.67 (d, 1H, J=2.1 Hz), 7.84 (d, 1H, J=8.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06756395B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-552ff75ebe944761a6c6c026da337dcb |
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| Source note | uspto-grants-2004_06 |
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