HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 23450598, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Butanal | HCID 261 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | 4-Hydroxy-2,2,6,6-tetramethylpiperidine | HCID 75471 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 23450598 | HCID 23450598 | — |
Reaction Steps
1.8 g 2,2,6,6-tetramethyl-piperidin-4-ol (intermediate product of Ciba Specialty Chemicals Inc.) are suspended in 7 ml of toluene. 3.6 ml of a 30% aqueous hydrogen peroxide solution and 0.41 g acetic acid are added at 5° C. and the solution is stirred at room temperature over night. 4.2 ml butanal and, after 15 min., 50 mg CuCl are added. The reaction mixture is stirred for 18 h at room temperature. The two phases are separated and the organic one is washed with 0.05M hydrochloric acid, sodium bisulfite solution, water, diluted sodium hydroxide solution, water and finally saturated sodium chloride solution. The organic phase is dried over sodium sulfate and finally evaporated to complete dryness under vacuum to afford 0.38 g product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08471031B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-631e4ad7df844a0ab26e16e0a957be37 |
| Source note | uspto-grants-2013_06 |