Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Tinuvin 770 | HCID 164282 | — |
| Catalyst | Molybdenum trioxide | HCID 14802 | — |
| Solvent | Octane | HCID 356 | — |
| Product | Tinuvin 123 | HCID 3592789 | 160.5% |
Reaction Steps
70% Aqueous tert-butyl hydroperoxide (140 g, 1.09 mol) is added over a 6-hour period to a mixture of 75.4 g (0.157 mol) of bis(2,2,6,6-tetramethylpiperidin-4-yl) sebacate, 1.25 g (8.7 mmol) of molybdenum trioxide and 570 ml of n-octane, that is first heated to 115° C., under a nitrogen atmosphere. During the addition, the reaction mixture is maintained at reflux. Water is collected in a Dean-Stark trap. Upon completion of the addition, the red reaction mixture is heated at reflux (95°-97° C.) for seven hours to discharge the red color. The molybdenum trioxide is removed by filtration. The yellow filtrate is stirred at ambient temperature for 30 minutes with 15 g of activated charcoal (DARCO) to remove some of the yellow color before being concentrated under reduced pressure. The crude product is purified by flash chromatography on silica gel (100:3 heptane:ethyl acetate) to afford 92.9 g (80% yield) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04921962 |
|---|
| Source dataset | uspto-grants-1990_05 |
|---|
| ORD ID | ord-e89ee52be7ca4ac3901581bda23aa2f7 |
|---|
| Source note | uspto-grants-1990_05 |
|---|