HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1-Methyl-2,6,7-trioxabicyclo[2.2.2]octan-4-yl)methanol → 4-Carboxy-1-methyl-2,6,7-trioxabicyclo[2.2.2]octane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1-Methyl-2,6,7-trioxabicyclo[2.2.2]octan-4-yl)methanol | HCID 13547990 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Carboxy-1-methyl-2,6,7-trioxabicyclo[2.2.2]octane | HCID 19936249 | — |
Reaction Steps
To a solution of 4-(hydroxymethyl)-1-methyl-2,6,7-trioxabicyclo[2.2.2]octane (10.0 g, 0.062 mol) in 200 mL of acetone is added Jones reagent (chromium trioxide and sulfuric acid) until an orange color persisted. The excess oxidant is removed by the addition of 2-propanol until a green color is obtained and the solvents are evaporated under reduced pressure. The residue is partitioned between dichloromethane (100 mL) and water (50 mL) and the layers are separated. The organic layer is washed with water, dried over anhydrous sodium sulfate and evaporated under reduced pressure to give 4-carboxy-1-methyl-2,6,7-trioxabicyclo[2.2.2]octane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05417959 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-d4c714964b194172822a3fb5f67121e7 |
| Source note | uspto-grants-1995_05 |