HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,6,6-Tetramethyl-4-piperidone → HCID 131711454, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,6,6-Tetramethyl-4-piperidone | HCID 13220 | — |
| Reactant | Diethyl (aminomethyl)phosphonate | HCID 1596920 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131711454 | HCID 131711454 | — |
Reaction Steps
31.0 g (0.21 mol) of triacetonamine and 33.4 g (0.20 mol) of diethyl aminomethylphosphonate are dissolved in 500 ml of ethanol, and the solution is hydrogenated, with the addition of 3 g of platinum-on-charcoal (containing 5% of platinum) and 3 drops of concentrated sulphuric acid, under a slight excess pressure until the absorption of hydrogen has ceased. The catalyst is filtered off and the filtrate is distilled. In this way is obtained diethyl (2,2,6,6-tetramethyl-4-piperidyl)-aminomethylphosphonate as a fine fraction which boils, under a pressure of 0.35 mm Hg, at a temperature of 130°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04144224 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-c385eb8c35774dc9960a340015d3c792 |
| Source note | uspto-grants-1979_03 |