HuagongsheHuagongshe Chemistry Print Report · For research reference only
Camphene → exo-3,3-Dimethylbicyclo(2.2.1)heptane-2-propionic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Camphene | HCID 6616 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Di-tert-butyl peroxide | HCID 8033 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | exo-3,3-Dimethylbicyclo(2.2.1)heptane-2-propionic acid | HCID 6455393 | — |
Reaction Steps
To refluxing acetic anhydride (1050 g., 10 moles), there is added dropwise over six hours a solution of camphene (136 g., 1 mole) and di-tert-butyl peroxide (0.1 mole, 14.6 g.). After complete addition, the mixture is heated at reflux for five hours. The cooled reaction mixture is concentrated under reduced pressure to leave a yellow-orange residual oil, 750 ml. of 2.5N NaOH is added to the residue which is then heated on the steam bath for one hour. The cooled solution is extracted once with ether, made acidic with concentrated HCl, and extracted thoroughly with ether. The dried (Na2SO4) ether extracts are concentrated under reduced pressure and the residue distilled under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04139559 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-00737a1b7cbd4f5b838dec7cf12cd5bb |
| Source note | uspto-grants-1979_02 |