4-(Trifluoromethyl)benzaldehyde → 4-Iodomethyl-5-isopropyl-2-(4-trifluoromethylphenyl)-oxazole
Reaction equation
[I:1][CH2:2][C:3]1[N:4]=C(C2C=CC(C)=CC=2)O[C:7]=1[C:8]1[CH:13]=CC=C[CH:9]=1.CC(C)C(=O)C(=NO)C.[F:30][C:31]([F:41])([F:40])[C:32]1[CH:39]=[CH:38][C:35]([CH:36]=[O:37])=[CH:34][CH:33]=1>>[I:1][CH2:2][C:3]1[N:4]=[C:36]([C:35]2[CH:38]=[CH:39][C:32]([C:31]([F:40])([F:41])[F:30])=[CH:33][CH:34]=2)[O:37][C:7]=1[CH:8]([CH3:13])[CH3:9]Participants
4
Procedure
Analogously to the building block synthesis of 4-iodomethyl-5-phenyl-2-p-tolyloxazole, 4-methylpentane-2,3-dione-2-oxime and 4-trifluoromethylbenzaldehyde gave 4-iodomethyl-5-isopropyl-2-(4-trifluoromethylphenyl)-oxazole.
Sources & evidence
- ORD record
- ord-e81abe1a742343c19dc9bd5c16844de6
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07365084B2
Reaction notes
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