HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70258Generated: October 26, 2026
Trifluoroacetic acid → Ethyl 5-{3-[(2-oxoethyl)oxy]phenyl}-2-thiophenecarboxylate
https://huagongshe.com/reaction/70258
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 58276762 | HCID 58276762 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | Ethyl 5-{3-[(2-oxoethyl)oxy]phenyl}-2-thiophenecarboxylate | HCID 86641430 | — |
Reaction Steps
Ethyl 5-(3-{[2,2-bis(ethyloxy)ethyl]oxy}phenyl)-2-thiophenecarboxylate (Intermediate KK-2-3) (1.41 g, 3.87 mmol) was dissolved in 20 ml of chloroform and cooled to 0° C. 5 ml of 50% aqueous trifluoroacetic acid solution was added. The mixture was stirred for 15 h at room temperature and 6 h at 65° C., cooled, diluted with chloroform and neutralized with saturated sodium bicarbonate solution. The organic layer was separated, washed with brine, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography (10 to 50% ethyl acetate in hexanes) to afford the title compound as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822518B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-4c98665bd16a49c597e8b882cfa24aab |
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| Source note | uspto-grants-2014_09 |
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