HCID 19965667, compound → HCID 86750605, compound
Reaction equation
[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:4][C:3]=1/[CH:13]=[CH:14]/[C:15]1[CH:20]=[CH:19][C:18](/[CH:21]=[CH:22]/[CH2:23][OH:24])=[CH:17][CH:16]=1>[O-2].[O-2].[Mn+4]>[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)=[N:4][C:3]=1[CH:13]=[CH:14][C:15]1[CH:16]=[CH:17][C:18](/[CH:21]=[CH:22]/[CH:23]=[O:24])=[CH:19][CH:20]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
(E,E)-3-[4-[2-(5-Methyl-2-phenyl-4-oxazolyl)vinyl]phenyl]-2propenol was oxidized with activated manganese dioxide in the same manner as in Reference Example 25 to yield (E)-4-[2-(5-methyl-2-phenyl-4-oxazolyl)vinyl]cinnamaldehyde, which was then recrystallized from ethyl acetate to yield light yellow prisms having a melting point of 191°-192° C.
Sources & evidence
- ORD record
- ord-c497d9b880db49228675b7b12f511b57
- Source dataset
- uspto-grants-1997_03
- Patent number
- US05614544
Reaction notes
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