Sodium Hydroxide → HCID 54513144, compound
Reaction equation
[C:1]1([C:7]2[N:8]=[C:9]([CH:18]=[CH:19][C:20]3[CH:21]=[C:22]([CH:26]=[CH:27][C:28]([O:30]CC)=[O:29])[CH:23]=[CH:24][CH:25]=3)[O:10][C:11]=2[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+]>>[C:1]1([C:7]2[N:8]=[C:9]([CH:18]=[CH:19][C:20]3[CH:21]=[C:22]([CH:26]=[CH:27][C:28]([OH:30])=[O:29])[CH:23]=[CH:24][CH:25]=3)[O:10][C:11]=2[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Procedure
Hydrolysis of ethyl 3-[3-[2-(4,5-diphenyl-2-oxazolyl)ethenyl]phenyl]-2-propenoate with sodium hydroxide analogously to the procedure of Example 10 provides the title compound.
Sources & evidence
- ORD record
- ord-b3ac9ba3a96949699bf384dbe75cd98b
- Source dataset
- uspto-grants-1993_11
- Patent number
- US05262540
Reaction notes
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