HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl hydroperoxide → 4-Acetamido-1-cyclohexyloxy-2,2,6,6-tetramethylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | 4-Acetamido-TEMPO | HCID 518988 | — |
| Catalyst | Molybdenum trioxide | HCID 14802 | — |
| Product | 4-Acetamido-1-cyclohexyloxy-2,2,6,6-tetramethylpiperidine | HCID 23372120 | — |
Reaction Conditions
| Temperature | 140 °C |
|---|
Reaction Steps
A stirred mixture of 10.0 g of 4-acetamido-2,2,6,6-tetramethylpiperidine-1-oxyl, 16 ml of 70% aqueous tert-butylhydroperoxide and 0.67 g of molybdenum trioxide in 75 ml of cyclohexane is heated under reflux in a flask fitted with a Dean-Stark apparatus. After 6 ml of water is collected, the reaction mixture is transferred to a Fisher Porter apparatus and heated at 140° C. and 30 psi for 4 hours. The decolorized reaction mixture is filtered and the filtrate is washed with water, aqueous sodium sulfite, brine, dried (MgSO4) and concentrated to give 13.61 g of a white solid. Recrystallization from heptane affords 10.39 g of the title compound as a white crystalline solid, m.p. 140°-44° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05204473 |
| Source dataset | uspto-grants-1993_04 |
| ORD ID | ord-84b88c07723a4a56b68009f22fc110ed |
| Source note | uspto-grants-1993_04 |