HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl hydroperoxide → HCID 54457070, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | HCID 53929497 | HCID 53929497 | — |
| Catalyst | Molybdenum trioxide | HCID 14802 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 54457070 | HCID 54457070 | 143.5% |
Reaction Conditions
| Temperature | 140 °C |
|---|
Reaction Steps
A mixture of 35.0 g (78.7 mmol) of di-(2,2,6,6-tetramethyl-piperidin-4-yl) isophthalate, 47.3 g (472 mmol) of 90% aqueous t-butyl hydroperoxide, 2.0 g of molybdenum trioxide, and 300 ml of cyclohexane is heated two hours at 140° C. in a Fischer-Porter bottle. The red reaction mixture is treated with an additional 20.0 g (90%, 200 mmol) of t-butyl hydroperoxide and heated at 140° C. for 120 minutes to discharge the red color. The reaction mixture is cooled, filtered, and the filtrate is evaporated to an oil which is crystallized from ethanol to afford 36.2 g (72% yield) of a white solid, m.p. 135°-141° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04921962 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-61763392ab80444f9d502a4988e1710d |
| Source note | uspto-grants-1990_05 |