HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52665Generated: October 29, 2026
Hexamethyldisilazane → Lithium Hexamethyldisilazide
https://huagongshe.com/reaction/52665
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Lithium Hexamethyldisilazide | HCID 2733832 | — |
Reaction Steps
To a THF (1 ml) solution of hexamethyldisilazane (51 μl, 0.242 mmol), 0.14 ml of n-butyl lithium (1.56M, 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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616732 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-85e050642b61417294e0da504870d6ff |
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| Source note | uspto-grants-1997_04 |
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