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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58276762HCID 58276762—
SolventChloroformHCID 6212—
SolventSodium BicarbonateHCID 516892—
ProductEthyl 5-{3-[(2-oxoethyl)oxy]phenyl}-2-thiophenecarboxylateHCID 86641430—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822518B2
Source datasetuspto-grants-2014_09
ORD IDord-4c98665bd16a49c597e8b882cfa24aab
Source noteuspto-grants-2014_09