Acetylacetone → HCID 12128919, compound
Reaction equation
[F:1][C:2]([F:12])([F:11])[C:3]1[CH:10]=[CH:9][C:6]([CH:7]=O)=[CH:5][CH:4]=1.[CH3:13][C:14](=[O:19])[CH2:15][C:16](=[O:18])[CH3:17]>>[F:1][C:2]([F:12])([F:11])[C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[C:15]([C:14](=[O:19])[CH3:13])[C:16](=[O:18])[CH3:17])=[CH:5][CH:4]=1Participants
3
Procedure
4-Trifluoromethylbenzaldehyde (8,7 g) was condensed with 2,4-pentanedione (5,01 g) in a similar manner as described above. The crude product was crystallized from a mixture of ether-petroleum ether (1:1), mp 46°-48° C., yield 3.8 g (30%).
Workup
- customThe crude product was crystallized from a mixture of ether-petroleum ether (1:1), mp 46°-48° C., yield 3.8 g (30%)
Sources & evidence
- ORD record
- ord-f0c8f933fd054718b5237cd28bb405d7
- Source dataset
- uspto-grants-1994_02
- Patent number
- US05288750
Reaction notes
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