HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium amide → HCID 70507079, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium amide | HCID 24532 | — |
| Reactant | 4-Piperidinol, 1,2,2,6,6-pentamethyl- | HCID 75472 | — |
| Reactant | HCID 70506026 | HCID 70506026 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 70507079 | HCID 70507079 | — |
Reaction Steps
A solution of 7.5 g (0.022 mole) of ethyl 4-(2-oxo-1-azepinyl)-2,2,6,6-tetramethylpiperidin-1-ylacetate and 4.2 g (0.024 mole) of 1,2,2,6,6-pentamethylpiperidin-4-ol in 50 ml of xylene is heated for one hour at 120° C. in the presence of 0.1 g of lithium amide esterification catalyst. The xylene-ethanol azeotropic mixture is slowly distilled off using an oil bath held at 150° C. to heat the reaction vessel. After five hours, four drops of acetic acid is added to the reaction mixture and the xylene solvent is removed by distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04472547 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-96a066b4ca9249c29df1dbd4f1923a83 |
| Source note | uspto-grants-1984_09 |