HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Lithium Hexamethyldisilazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | HCID 13578039 | HCID 13578039 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Lithium Hexamethyldisilazide | HCID 2733832 | — |
Reaction Steps
A solution of lithium hexamethyldisilazide was prepared by the addition of 5.12 ml of a 1.6M solution of n-butyllithium in hexane to 1.75 ml of hexamethyldisilazane in 25 ml of dry THF at -10° with stirring, under argon. The solution was cooled to -78° and added to 1.0 g of methyl 2-(4-allylthioazetidin-2-on-1-yl)acetate in 12 ml of dry tetrahydrofuran at -78°, with stirring, under argon. After 5 min, 0.846 ml of carbon disulphide was added by syringe. 1.77 ml of acetic anhydride were then added, followed by 1.07 ml of glacial acetic acid. The solution was allowed to warm to room temperature and evaporated to leave a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04526718 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-3a895bd3c86244d9a069d2010d857a80 |
| Source note | uspto-grants-1985_07 |