HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl hydroperoxide → 2-Hexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | 1-Hexene | HCID 11597 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 2-Hexanone | HCID 11583 | — |
| Product | 1-Hexene | HCID 11597 | — |
Reaction Steps
30 cm3 of 80% tert-butyl hydroperoxide (0.225 mole), 10 cc of 1-hexene (0.064 mole), 20 cc of dichloroethane and 220 mg of palladium acetate (0.001 mole) are introduced into a heat-insulated glass reactor. An argon atmosphere is applied and stirring is performed at a temperature of 60° C. After 4 hours, it is found that 66% of 1-hexene were converted and that 2-hexanone was formed with a molar selectivity of 83% with respect to the converted 1-hexene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04310704 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-4a20c8b592214182aa0f60ef1a82cb7b |
| Source note | uspto-grants-1982_01 |