HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → (1R)-Camphoric anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Camphoric Acid | HCID 101807 | — |
| Product | (1R)-Camphoric anhydride | HCID 68989 | — |
Reaction Steps
A mixture of (1R-cis)-1,2,2-Trimethylcyclopentane-1,3-dicarboxylic acid)[(1R,3S)-camphoric acid](40.0 g), AcCl (23.5 g), and Ac2O (81.6 g) was heated under reflux for 3 hr. The mixture was concentrated in vacuo, dissolved in CHCl3, washed with sat. NaHCO3, brine, and dried over Na2SO4. The solvent was removed in vacuo and the residue was triturated with i-Pr2O to give (1R)-1,8,8-Trimethyl-3-oxabicyclo[3.2.1]octane-2,4-dione[(1R)-camphoric anhydride (34.0 g) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06482849B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-2fdf2d28283d4f589ca6e523c92ee28c |
| Source note | uspto-grants-2002_11 |