HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427024Generated: October 26, 2026
Potassium Carbonate → Ethyl 5-ethyl-2-(2-nitroanilino)-thiophene-3-carboxylate
https://huagongshe.com/reaction/427024
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | Ethyl 2-amino-5-ethyl-3-thenoate | HCID 78263 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Ethyl 5-ethyl-2-(2-nitroanilino)-thiophene-3-carboxylate | HCID 12442327 | — |
Reaction Steps
o-Fluoronitrobenzene (b 56.4 g, 0.4 mol) and ethyl 2-amino-5-ethylthiophene-3-carboxylate (100 g, 0.5 mol) were dissolved in dry dimethylsulphoxide (320 ml). The stirred solution, under nitrogen, was heated in an oil bath. When the internal temperature reached 60° C., potassium carbonate (55 g, 0.4 mol) was added and the mixture stirred at 100° C. until GLC indicated that all the o-fluoronitrobenzene had been consumed (6.5 hours). The mixture was then poured onto ice-water, acidified with concentrated hydrochloric acid and extracted with methylene chloride. The combined extracts were washed with water, dried (MgSO4) and the solvent evaporated to give a red semi-solid which was recrystallised from ethanol to give the title product as a solid (m.p. 66°-68° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04172831 |
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| Source dataset | uspto-grants-1979_10 |
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| ORD ID | ord-24a0ebf52c4b446781ca2e07a5a57159 |
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| Source note | uspto-grants-1979_10 |
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