HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986647Generated: October 27, 2026
Methyl 7-nitrobenzo[b]thiophene-2-carboxylate → Methyl 7-amino-1-benzothiophene-2-carboxylate
https://huagongshe.com/reaction/1986647
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 7-nitrobenzo[b]thiophene-2-carboxylate | HCID 57722418 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | Methyl 7-amino-1-benzothiophene-2-carboxylate | HCID 45089769 | 100% |
Reaction Steps
To a mixture of 7-nitro-benzo[b]thiophene-2-carboxylic acid methyl ester (100 mg) in acetic acid (4 mL) was added a solution of SnC2.2H2O (10 eq) in 1.5 mL of concentrated HCl. The reaction was stirred at room temperature 12 h. The excess acid was partially removed in vacuo, and the reaction mixture was then poured into a flask (250 mL) and was neutralized with saturated NaHCO3 solution at 0° C. The pH was brought up to pH 9 by adding solid NaHCO3. The resulting aqueous mixture was diluted with EtOAc, and the Tin-by product was removed by filtering through a pad of diatomaceous earth. The pad was rinsed with EtOAc and the combined filtrates were partitioned in a separatory funnel. The aqueous layer was extracted with EtOAc two times times. The combined organics were dried over MgSO4, filtered and concentrated to give the desired 7-amino-benzo[b]thiophene-2-carboxylic acid methyl ester (100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07550461B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-3be63abe472f44f9b1eb7d94f1922fc9 |
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| Source note | uspto-grants-2009_06 |
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