HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 2,2,6,6-Tetramethyl-4-piperidone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Acetonin | HCID 68396 | — |
| Catalyst | Phenylhydrazine hydrochloride | HCID 60962 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,2,6,6-Tetramethyl-4-piperidone | HCID 13220 | 75% |
Reaction Steps
A flask with attached condenser was charged with 80 g of acetonine, 80 g of acetone, 16 g methanol and 1.6 g N-phenylhydrazine monohydrochloride and the mixture reacted at 50°-55° C. for 18 hours, while stirring. The reaction solution was stripped under reduced pressure, to obtain a light red residue. This residue was distilled in vacuo to obtain 60.4 g of triacetonamine. White crystals were obtained by recrystallization from petroleum ether having the melting point of 34°-36° C. The compound was confirmed to be the objective matter by IR spectrum and gas chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04252958 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-db6825e056c74d1485fbc90964a0eb00 |
| Source note | uspto-grants-1981_02 |