HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779326Generated: October 31, 2026
Sodium hydride → Methyl 5-methyl-2-((2-nitrophenyl)amino)thiophene-3-carboxylate
https://huagongshe.com/reaction/1779326
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | Methyl-2-amino-5-methyl-3-thiophenecarboxylate | HCID 675878 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 5-methyl-2-((2-nitrophenyl)amino)thiophene-3-carboxylate | HCID 19592005 | — |
Reaction Steps
To a stirred suspension of sodium hydride (2 g) in dry tetrahydrofuran (25 mL) under a nitrogen atmosphere was added a solution of methyl 2-amino-5-methylthiophene-3-carboxy-late (4.8 g, 0.028 mol) and 2fluoronitrobenzene (4.0 g, 0.025 mol) in dry tetrahydrofuran (30 mL). The mixture was stirred at 25° C. for 20 hours, poured onto ice and partitioned between 2N hydrochloric acid and ethyl acetate. The organic extracts were dried over magnesium sulfate, the solvent was evaporated under reduced pressure and the title compound purified by chromatography on silica gel, eluted with toluene, and crystallized from ethanol (4.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05627178 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-12243d81505040f181931c35e2206fe9 |
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| Source note | uspto-grants-1997_05 |
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