HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanone → 12,14-Dihydroxy-3-oxocard-20(22)-enolide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Aluminum isopropoxide | HCID 11143 | — |
| Reactant | Digoxigenin | HCID 15478 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 12,14-Dihydroxy-3-oxocard-20(22)-enolide | HCID 20503 | 189.5% |
Reaction Steps
A mixture of 488 mg digoxigenin, 7.5 ml toluene, 3.75 ml cyclohexanone, and 550 mg aluminum isopropoxide was heated under reflux for 2.3 hours and then concentrated in vacuo to half of its original volume. Two hundred μl water was added and the mixture was evaporated in vacuo to dryness. The powdery solid was dried in vacuo over overnight. The dry residue was stirred in 25 ml methanol and the resulting mixture was filtered. The residue on the funnel was washed with 25 ml methanol. The filtrate and washing were combined and evaporated in vacuo affording 920 mg white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06060598 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-ba373593c86540c2b28bede3a478d518 |
| Source note | uspto-grants-2000_05 |