Reaction equation
[CH3:1][N:2]1[C@@H:19]2[CH2:20][C:7]3[CH:8]=[CH:9][C:10]([O:21][CH3:22])=[C:11]4[O:12][C@H:13]5[C:14]([CH:16]=[CH:17][C@@H:18]2[C@:5]5([C:6]=34)[CH2:4][CH2:3]1)=[O:15].[C:23]([O:26][OH:27])(=[O:25])[CH3:24]>CCOCC>[CH3:1][N:2]1[C@@H:19]2[CH2:20][C:7]3[CH:8]=[CH:9][C:10]([O:21][CH3:22])=[C:11]4[O:12][CH:13]5[C:14]([CH:16]=[CH:17][C@:18]2([OH:25])[C@:5]5([C:6]=34)[CH2:4][CH2:3]1)=[O:15].[C:23]([O:26][OH:27])(=[O:25])[CH3:24]Participants
5
Procedure
14-Hydroxycodeinone was synthesized from the dienolsilyl ether of codeinone by oxidative hydroxylation using a peracetic acid solution preparation. The peracetic acid solution was prepared as follows:
Sources & evidence
- ORD record
- ord-380c0706ce624b569b2a107fe5673d80
- Source dataset
- uspto-grants-2001_01
- Patent number
- US06177567B1
Linked notes
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