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 | 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 32.9 ml of a 1.6M solution of n-butyllithium in hexane to 11.25 ml of hexamethyldisilazane in 125 ml of dry THF at -10° with stirring, under argon. The solution was cooled to -78° and added to 5.0 g of methyl 2-(4-allylthioazetidin-2-on-1-yl)acetate in 60 ml of dry tetrahydrofuran at -78°, with stirring, under argon. After 5 min, 4.23 ml of carbon disulphide was added by syringe. 885 ml of acetic anhydride was then added. The solution were 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-c1b25808bb8a47158ce43019585d4a18 |
| Source note | uspto-grants-1985_07 |