HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → 1-Methoxy-2,2,6,6-tetramethylpiperidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | 2,2,6,6-Tetramethyl-4-piperidone | HCID 13220 | — |
| Catalyst | Sodium tungstate | HCID 26052 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Product | 1-Methoxy-2,2,6,6-tetramethylpiperidin-4-one | HCID 10976193 | 64% |
Reaction Steps
The intermediate, 1-oxy-2,2,6,6-tetramethyl-piperidin-4-one, can be produced by reacting 2,2,6,6-tetramethyl-piperidin-4-one with 1.75 equivalents of hydrogen peroxide in 2M sodium chloride solution, with 1 mol % sodium tungstate added, for 12 h at 50°. When the reaction is complete, the solution is slightly acidified with 2 N hydrochloric acid to pH 5, then 3 equivalents of acetaldehyde and two equivalents of 30% hydrogen peroxide are added slowly at 50°. The mixture is stirred at 90° for 2 h, and then cooled. The work-up, as above in example E, gives 64% of liquid product, crystallizes slowly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08471031B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-205d12e2811747b6ae27764c06788ff0 |
| Source note | uspto-grants-2013_06 |