HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483968Generated: October 25, 2026
Sodium hydride → Methyl 5-methyl-2-((2-nitrophenyl)amino)thiophene-3-carboxylate
https://huagongshe.com/reaction/483968
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-carboxylate (4.8 g, 0.028 mol) and 2-fluoronitrobenzene (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 sulphate, the solvent was evaporated under reduced pressure and the title compound purified by chromatography on silica gel, eluted with toluene, and crystallised from ethanol (4.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05229382 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-308d214c725e4e9d8c68673f1534a0a4 |
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| Source note | uspto-grants-1993_07 |
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