Lithium Hydroxide → HCID 58319216, compound
Reaction equation
C([O:3][C:4]([C:6]1[N:7]=[C:8]([CH2:11][C:12]2[CH:17]=[CH:16][C:15]([C:18]([CH3:21])([CH3:20])[CH3:19])=[CH:14][CH:13]=2)[S:9][CH:10]=1)=[O:5])C.[Li+].[OH-]>>[C:18]([C:15]1[CH:16]=[CH:17][C:12]([CH2:11][C:8]2[S:9][CH:10]=[C:6]([C:4]([OH:5])=[O:3])[N:7]=2)=[CH:13][CH:14]=1)([CH3:21])([CH3:19])[CH3:20]Participants
3
Procedure
2-(4-tert-Butylbenzyl)thiazole-4-carboxylic acid ethyl ester was hydrolysized with 1M LiOH (5 ml). The reaction solvent was removed in vacuo. The residue was diluted with EtOAc and H2O and the aqueous layer was extracted with EtOAc. The combined organic layer was washed with brine, dried over MgSO4 and then concentrated in vacuo.
Workup
- customThe reaction solvent was removed in vacuo
- additionThe residue was diluted with EtOAc and H2O
- extractionthe aqueous layer was extracted with EtOAc
- washThe combined organic layer was washed with brine
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-3937f935990d4bfc9c1e93157c128713
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08691855B2
Reaction notes
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