Sodium Hydroxide → sodium 3-[4-[[4-[(2Z)-2-methoxyimino-2-phenylethoxy]phenyl]methoxy]phenyl]-3-(1,2-oxazol-3-yl)propanoate
Reaction equation
[CH3:1][O:2]/[N:3]=[C:4](/[C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)\[CH2:5][O:6][C:7]1[CH:30]=[CH:29][C:10]([CH2:11][O:12][C:13]2[CH:18]=[CH:17][C:16]([CH:19]([C:24]3[CH:28]=[CH:27][O:26][N:25]=3)[CH2:20][C:21]([OH:23])=[O:22])=[CH:15][CH:14]=2)=[CH:9][CH:8]=1.[OH-].[Na+:38]>>[CH3:1][O:2]/[N:3]=[C:4](/[C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)\[CH2:5][O:6][C:7]1[CH:8]=[CH:9][C:10]([CH2:11][O:12][C:13]2[CH:18]=[CH:17][C:16]([CH:19]([C:24]3[CH:28]=[CH:27][O:26][N:25]=3)[CH2:20][C:21]([O-:23])=[O:22])=[CH:15][CH:14]=2)=[CH:29][CH:30]=1.[Na+:38]Participants
3
Procedure
Compound 29 was synthesized from 3-{4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-3-(1,2-oxazol-3-yl)propanoic acid (0.07 g, 0.14 mmol) and sodium hydroxide (0.0057 g, 0.14 mmol) by following the procedure described in scheme 12 (0.052 g, yield: 71.2%); Purity: 99.00%.
Sources & evidence
- ORD record
- ord-bfb9ebaa29c34190b9d708d4b4916855
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09278915B2
Reaction notes
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