HCID 19965621, compound → HCID 19965663, compound
Reaction equation
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[O:7][C:8]([CH3:25])=[C:9](/[CH:11]=[CH:12]/[C:13]2[CH:18]=[CH:17][C:16](/[CH:19]=[CH:20]/[CH:21]=[CH:22]/[CH2:23][OH:24])=[CH:15][CH:14]=2)[N:10]=1>[O-2].[O-2].[Mn+4]>[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[O:7][C:8]([CH3:25])=[C:9](/[CH:11]=[CH:12]/[C:13]2[CH:14]=[CH:15][C:16](/[CH:19]=[CH:20]/[CH:21]=[CH:22]/[CH:23]=[O:24])=[CH:17][CH:18]=2)[N:10]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
(E,E,E)-5-[4-[2-[2-(2-Furyl)-5-methyl-4-oxazolyl]vinyl]phenyl]-2,4-pentadien-1-ol was oxidized with activated manganese dioxide in the same manner as in Reference Example 25 to yield (E,E,E)-5-[4-[2-[2-(2-furyl)-5- methyl-4-oxazolyl]vinyl]phenyl]-2,4-pentadien-1-al, which was then recrystallized from ethyl acetate to yield light brown prisms having a melting point of 179°-180° C.
Sources & evidence
- ORD record
- ord-e2ec6a7754b74e0bbc0a23fbc2189f9a
- Source dataset
- uspto-grants-1997_03
- Patent number
- US05614544
Reaction notes
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