Trifluoroacetic acid → HCID 178470134, compound
Reaction equation
[OH:1][C:2]1[C:11]2[C:6](=[C:7]([F:14])[C:8]([F:13])=[C:9]([F:12])[CH:10]=2)[N:5]=[C:4]([S:15]CC2C=CC(OC)=CC=2)[C:3]=1[C:25]([O:27][CH2:28][CH3:29])=[O:26].FC(F)(F)C(O)=O.FC(F)(F)S(O)(=O)=O.C1(OC)C=CC=CC=1>>[OH:1][C:2]1[C:11]2[C:6](=[C:7]([F:14])[C:8]([F:13])=[C:9]([F:12])[CH:10]=2)[N:5]=[C:4]([SH:15])[C:3]=1[C:25]([O:27][CH2:28][CH3:29])=[O:26]Participants
Procedure
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.).
Workup
- stirringThe mixture was stirred at -20° to -15° C. for 30 minutes
- waitat room temperature for 1.5 hour
- concentrationAfter the reaction mixture was concentrated under reduced pressure
- additiona piece of ice was added to the
- concentrationconcentrate
- customAfter insoluble materials were removed by filtration
- washthe filtrate was washed with ether
- filtrationThe resulting powder was filtered
Sources & evidence
- ORD record
- ord-ffa11bc1976c4e4da69c0d2c747e0fef
- Source dataset
- uspto-grants-1989_08
- Patent number
- US04853469
Reaction notes
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