4-Methylbenzaldehyde → 2-(4-Methylphenyl)-4-iodomethyl-5-methyloxazole
Reaction equation
[I:1][CH2:2][C:3]1[N:4]=[C:5]([C:14]2[CH:19]=[CH:18][C:17]([CH3:20])=[CH:16][CH:15]=2)[O:6][C:7]=1[C:8]1C=CC=CC=1.C/C(/C(C)=O)=N\O.C1(C)C=CC(C=O)=CC=1>>[I:1][CH2:2][C:3]1[N:4]=[C:5]([C:14]2[CH:19]=[CH:18][C:17]([CH3:20])=[CH:16][CH:15]=2)[O:6][C:7]=1[CH3:8]Participants
4
Procedure
Analogously to the building block synthesis of 4-iodomethyl-5-phenyl-2-p-tolyloxazole, diacetylmonoxime and p-tolualdehyde gave 4-iodomethyl-5-methyl-2-p-tolyloxazole.
Sources & evidence
- ORD record
- ord-5afcce69d7ef41deb79faca853bf5de9
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07259177B2
Reaction notes
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