3-(Trifluoromethyl)benzaldehyde → 4-Iodomethyl-5-isopropyl-2-(3-trifluoromethylphenyl)-oxazole
Reaction equation
[I:1][CH2:2][C:3]1[N:4]=[C:5]([C:14]2[CH:19]=[CH:18][C:17](C)=[CH:16][CH:15]=2)[O:6][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])C1C=C(C=CC=1)C=O>>[I:1][CH2:2][C:3]1[N:4]=[C:5]([C:14]2[CH:15]=[CH:16][CH:17]=[C:18]([C:31]([F:41])([F:40])[F:30])[CH:19]=2)[O:6][C:7]=1[CH:8]([CH3:9])[CH3:13]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 3-trifluoromethylbenzaldehyde gave 4-iodomethyl-5-isopropyl-2-(3-trifluoromethylphenyl)-oxazole.
Sources & evidence
- ORD record
- ord-18c65215853846b9b5cb4780e1ec53f0
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07365084B2
Reaction notes
Loading…