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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722072Generated: October 27, 2026

Trifluoroacetic acid → HCID 178470134, compound

https://huagongshe.com/reaction/1722072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantHCID 178470096HCID 178470096—
ProductHCID 178470134HCID 17847013476.9%

Reaction Steps

Ethyl 4-hydroxy-6,7,8-trifluoro-2-(p-methoxybenzylthio)quinoline-3-carboxylate (59.9 g) was added to a mixture of trifluoroacetic acid (500 g), trifluoromethanesulfonic acid (100 g) and anisole (92.5 g) at -23° to -20° C. with stirring over a period of 15 minutes. The mixture was stirred at -20° to -15° C. for 30 minutes and then at room temperature for 1.5 hour. After the reaction mixture was concentrated under reduced pressure, a piece of ice was added to the concentrate and the mixture was made alkaline with 10% aqueous sodium hydroxide. After insoluble materials were removed by filtration, the filtrate was washed with ether and made strongly acidic with concd. hydrochloric acid. The resulting powder was filtered to give the title compound (33 g), which was recrystallized from ethanol to give yellow crystals, m.p. 190° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04853469
Source datasetuspto-grants-1989_08
ORD IDord-ffa11bc1976c4e4da69c0d2c747e0fef
Source noteuspto-grants-1989_08