4'-Fluoroacetophenone → 4-Fluorophenylglyoxal hydrate
Reaction equation
O.[C:2]1([C:8]([CH:10]=[O:11])=[O:9])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[F:12]C1C=CC(C(=O)C)=CC=1>>[OH2:9].[F:12][C:5]1[CH:6]=[CH:7][C:2]([C:8]([CH:10]=[O:11])=[O:9])=[CH:3][CH:4]=1Participants
3
Procedure
The title compound was prepared using essentially the same procedure as described by H. A. Riley and A. R. Gray in Organic Synthesis, Collective Volume II, p. 509 for the preparation of phenylglyoxal hydrate, but using 4′-fluoroacetophenone in place of acetophenone.
Sources & evidence
- ORD record
- ord-518d1a45cbd74b60a796d8dc569cf6db
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06727244B2
Reaction notes
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