HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591552Generated: October 30, 2026
Trifluoroacetic anhydride → Methyl 3-(2-ethoxy-2-oxoethoxy)thieno[2,3-b]pyridine-2-carboxylate 7-oxide
https://huagongshe.com/reaction/591552
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Carbamide Peroxide | HCID 31294 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 3-(2-ethoxy-2-oxoethoxy)thieno[2,3-b]pyridine-2-carboxylate | HCID 1478603 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 3-(2-ethoxy-2-oxoethoxy)thieno[2,3-b]pyridine-2-carboxylate 7-oxide | HCID 118656082 | 46.7% |
Reaction Steps
To a mixture of methyl 3-(2-ethoxy-2-oxoethoxy)thieno[2,3-b]pyridine-2-carboxylate (500 mg), urea hydrogen peroxide (239 mg) and CH3CN (8 mL) was added TFAA (0.353 mL) at room temperature. The mixture was stirred at room temperature for 4 h and at 70° C. overnight. To the mixture were added urea hydrogen peroxide (80 mg) and TFAA (0.118 mL). The mixture was stirred at 70° C. for 2 h. After cooling, to the mixture was added saturated aqueous NaHCO3. The resulting precipitate was collected by filtration to give the title compound (246 mg). The filtrate was concentrated. The residue was extracted with EtOAc. The combined organic layer was washed with brine, dried over MgSO4 and concentrated in vacuo to give the title compound (85.1 mg). Total yield: 331 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238639B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-eb6256c6f12e408ca9166d15ba79132f |
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| Source note | uspto-grants-2016_01 |
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