HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl hydroperoxide → HCID 20222582, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Sodium Phosphate, Dibasic | HCID 24203 | — |
| Reactant | HCID 20222602 | HCID 20222602 | — |
| Catalyst | Molybdenum carbonyl (Mo(CO)6) | HCID 98885 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 20222582 | HCID 20222582 | — |
Reaction Steps
35 g of a hydrocarbon mixture containing (according to GC) 43% of 1,1,4,4-tetramethyl-1,2,3,4,5,8-hexahydronaphthalene (IIh) are dissolved in 140 ml of 1,2-dichloroethane and treated in accordance with method C described in Example 1 with 0.304 g of molybdenum hexacarbonyl, 0.1148 g of disodium hydrogen phosphate and 65 ml of 2.85 molar tert.butyl hydroperoxide solution. After working-up, 30 g of crude product are obtained. 10 g thereof are chromatographed on 600 g of silica gel Merck (0.04-0.063 mm) (elution agent: 2-3% ether/hexane). 1.9 g of 6,7-epoxy-1,1,4,4-tetramethyl-1,2,3,4,5,6,7,8-octahydro-naphthalene are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04634548 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-aa8dea30ed08411cb111bd81bde696c9 |
| Source note | uspto-grants-1987_01 |