p-Toluenesulfonic acid → Ethyl 2-ethyl-3,4,5,6-tetrafluorobenzoylacetate
Reaction equation
[CH2:1]([C:3]1[C:21]([F:22])=[C:20]([F:23])[C:19]([F:24])=[C:18]([F:25])[C:4]=1[C:5]([CH:7](C(OCC)=O)[C:8]([O:10][CH2:11][CH3:12])=[O:9])=[O:6])[CH3:2].C1(C)C=CC(S(O)(=O)=O)=CC=1>>[CH2:1]([C:3]1[C:21]([F:22])=[C:20]([F:23])[C:19]([F:24])=[C:18]([F:25])[C:4]=1[C:5]([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])=[O:6])[CH3:2]Participants
3
Procedure
Employing diethyl 2-ethyl-3,4,5,6-tetrafluorobenzoylmalonate (17.2 g) and p-toluenesulfonic acid (0.25 g), the procedure of Reference Example 19 is repeated to give ethyl 2-ethyl-3,4,5,6-tetrafluorobenzoylacetate (11.09 g).
Sources & evidence
- ORD record
- ord-083033d09e64409f848f83a084612e1d
- Source dataset
- uspto-grants-1996_02
- Patent number
- US05495020
Reaction notes
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