Reaction equation
C[Si]([N-][Si](C)(C)C)(C)C.[K+].[C:11]1([C@H:17]2[CH2:21][O:20][C:19](=[O:22])[N:18]2[C:23](=[O:33])[CH2:24][C@@H:25]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[CH3:26])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C(C1C=C(C(C)C)C=C(C(C)C)C=1S([N:52]=[N+:53]=[N-:54])(=O)=O)(C)C.C(O)(=O)C>O1CCCC1.O>[N:52]([C@@H:24]([C@@H:25]([C:27]1[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=1)[CH3:26])[C:23]([N:18]1[C@@H:17]([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH2:21][O:20][C:19]1=[O:22])=[O:33])=[N+:53]=[N-:54]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
Potassium bis(trimethylsilyl)amide (2.0 mL, 1.8 mmol, 0.91 M in tetrahydrofuran) was added to (S)-4-phenyl-3-((S)-3-phenyl-butyryl)-oxazolidin-2-one (500 mg, 1.6 mmol) in anhydrous tetrahydrofuran (8 mL) at −78° C. and stirred for 1 hour. In a separate flask, a solution of 2,4,6-triisopropylbenzenesulphonyl azide (625 mg, 2.0 mmol) in anhydrous tetrahydrofuran (10 mL) at −78° C. was added via cannula to the anion at −78° C. and stirring continued for 2 hours. Acetic acid (0.45 mL, 7.8 mmol) was added to the reaction at −78° C., the mixture warmed to room temperature and stirred overnight. The mixture was poured into water (30 mL) and extracted with ethyl acetate. The combined extracts were washed with brine and dried over sodium sulfate. The crude product was purified on silica gel with 2:1 dichloromethane/hexane to give (S)-3-((2S,3R)-2-azido-3-phenyl-butyryl)-4-phenyl-oxazolidin-2-one (230 mg, 41%).
Workup
- stirringstirring
- waitcontinued for 2 hours
- stirringstirred overnight
- extractionextracted with ethyl acetate
- washThe combined extracts were washed with brine
- dry with materialdried over sodium sulfate
- customThe crude product was purified on silica gel with 2:1 dichloromethane/hexane
Sources & evidence
- ORD record
- ord-63ca72f3d4f24e16ba1c51f65551f18a
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07427635B2
Linked notes
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