HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bis(acetoxy)iodobenzene → 4-tert-Butylcyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bis(acetoxy)iodobenzene | HCID 21865429 | — |
| Reactant | 2,6,6-Trimethyl-3,3-bis(2,6,6-trimethyl-3-bicyclo[3.1.1]hept-1-enyl)bicyclo[3.1.1]hept-1-ene | HCID 53472035 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-tert-Butylcyclohexanone | HCID 7392 | — |
Reaction Steps
To a 4-t-butylcyclohexane-1,1-dihydroperoxide and terpinene (trapping reagent) in a stirred room temperature solution of carbon tetrachloride was added, over a period of five to ten minutes, a solution of bisacetoxyiodobenzene (BAIB) in carbon tetrachloride. Rapid bubbling commenced upon addition of the BAIB solution and ceased within a few minutes after addition was completed. Stirring was continued for 0.5 h, after which the solution was filtered through a plug of silica, which was washed with CH2Cl2. The residue obtained upon concentration was purified by column chromatography on silica gel to give 4-t-butyl cyclohexanone and the trapping product ascaridole (endoperoxide of terpinene).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08182785B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-37ba5328c74f4ce7aa6f8813dc87a875 |
| Source note | uspto-grants-2012_05 |