HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 86594336, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ozone | HCID 24823 | — |
| Reactant | HCID 13583530 | HCID 13583530 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86594336 | HCID 86594336 | 40% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a solution of 3-methylenyl bicyclo[3,2,1]octan-8-one ethylene ketal (0.21 g, 1.15 mmol, 1.0 eq.) in CH2Cl2 (2 mL) at −78° C. was bubbled O3 until the reaction stayed blue (about 3 min). The O3 bubbling was stopped and the reaction mixture was stirred for 5 min at −78° C. The reaction was quenched by addition of triphenylphosphine (0.43 g, 1.4 eq.) and stirring at −78° C. for 10 minutes. The reaction mixture was allowed to warm at room temperature, stirred for 40 minutes and concentrated. The residue was purified by silica gel chromatography (10% to 15% EtOAc-hexanes) to give bicyclo[3,2,1]octane-3,8-dione 8-ethylene ketal as a colorless oil (0.08 g, 40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691814B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-fa0bd720f9bc478a803c31fafdea2632 |
| Source note | uspto-grants-2014_04 |