HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054231Generated: November 1, 2026
Methyl 3-amino-2-thiophenecarboxylate → Methyl 3-nitrothiophene-2-carboxylate
https://huagongshe.com/reaction/1054231
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 3-amino-2-thiophenecarboxylate | HCID 89652 | — |
| Reactant | Sodium Tetrafluoroborate | HCID 4343483 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 3-nitrothiophene-2-carboxylate | HCID 11137855 | 63% |
Reaction Steps
To a stirring solution of methyl 3-aminothiophene-2-carboxylate (5 g, 31.8 mmol) in Conc. HCl (4.77 ml) was added aq. solution of sodium nitrite (2.195 g, 31.8 mmol) slowly at 0-5° C. Reaction mixture was stirred at 0-5° C. for 1 h. To this was added aq. solution of sodium tetrafluoroborate (5.24 g, 47.7 mmol) in one lot. After 30 min. precipitated product was filtered. The product was added to the stirring suspension of copper bronze (6.06 g, 95 mmol) and sodium nitrite (26.3 g, 382 mmol) in water (100 ml). Reaction mixture was stirred at 25° C. for 1 h. Reaction mixture was diluted with water and EtOAc and filtered through Hyflow bed. The organic layer was separated and distilled out to get crude product which was column purified using 0-5% EtOAC in hexane to get titled compound as light yellow solid in 63% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394300B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-6133b796f30b426dab1c686e7820c60b |
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| Source note | uspto-grants-2016_07 |
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