Hexamethyldisilazane → Lithium Hexamethyldisilazide
Reaction equation
[CH3:1][Si:2]([CH3:9])([CH3:8])[NH:3][Si:4]([CH3:7])([CH3:6])[CH3:5].C([Li:14])CCC>C1COCC1>[CH3:1][Si:2]([CH3:9])([CH3:8])[N-:3][Si:4]([CH3:7])([CH3:6])[CH3:5].[Li+:14]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a THF (1 ml) solution of hexamethyldisilazane (51 μl, 0.242 mmol), 0.14 ml of n-butyl lithium (1.56 M, hexane solution) was added at -78° C., followed by stirring for 30 minutes to obtain a lithium hexamethyldisilazide solution. To this solution, a THF solution (2 ml) of 105 mg of (1S,5R,6R,7R)-2-oxa-7-t-butyldimethylsiloxy-6-{(3S,5S)-3-t-butyldimethylsiloxy-5-methyl-E-1-nonenyl}bicyclo[3.3.0]octan-3-one (Compound 32) was dropwise added at -78° C., and the mixture was stirred for 30 minutes. Then, 76.2 mg of N-fluorobenzenesulfonimide was added thereto at -78° C. The mixture was stirred at -78° C. for 15 minutes, at 0° C. for 30 minutes and at room temperature for 30 minutes and then poured into a saturated ammonium chloride aqueous solution, and the mixture was extracted with ethyl acetate. The extract was purified by silica gel column chromatography (ethyl acetate:hexane=1:30 to 1:10) to obtain 40 mg of the above-identified compound.
Sources & evidence
- ORD record
- ord-4ab8bb1215e54682975934eeab24ad68
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05538995
Reaction notes
Loading…