Sodium Hydroxide → HCID 10001657, compound
Reaction equation
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[N:7]=[C:8]([CH2:16][CH2:17][C:18]2[CH:19]=[C:20]([CH:27]=[CH:28][CH:29]=2)[O:21][CH2:22][C:23]([O:25]C)=[O:24])[O:9][C:10]=1[C:11]1[S:12][CH:13]=[CH:14][CH:15]=1.[OH-].[Na+]>>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[N:7]=[C:8]([CH2:16][CH2:17][C:18]2[CH:19]=[C:20]([CH:27]=[CH:28][CH:29]=2)[O:21][CH2:22][C:23]([OH:25])=[O:24])[O:9][C:10]=1[C:11]1[S:12][CH:13]=[CH:14][CH:15]=1Participants
3
Procedure
Hydrolysis of methyl [3-[2-[4,5-di(2-thienyl)-2-oxazolyl]ethyl]phenoxy]acetate with aqueous sodium hydroxide provided the hydrated title compound, m.p. 105.5°-107° C.
Sources & evidence
- ORD record
- ord-6a2b7fe7fc3344679ae0802d18bd9af4
- Source dataset
- uspto-grants-1993_11
- Patent number
- US05262540
Reaction notes
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