Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | (-)-Isopulegol | HCID 170833 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Coolact HK | HCID 10964760 | 34% |
Reaction Steps
(−)-Isopulegol (60 mg) was dissolved in DMF (4 mL), and OsO4 (0.05 mL, 2.5% in tBuOH) was added and stirred for 5 min. OXONE (0.235 g) was added in one portion and the reaction had a final volume (6 mL). The reaction was stirred at room temperature for 3 hours or until the solution becomes colorless. This usually marks the completion of the reaction which was verified by TLC or GC. Na2SO3 (360 mg) was added, to reduce the remaining Os(VIII), and stirred for an additional hour or until solution became dark brown/black. EtOAc was added to extract the products and 1N HCl was used to dissolve the salts. The organic extract was washed with 1N HCl (50 mL×3) and brine (50 mL), dried over Na2SO4, and the solvent was removed under reduced pressure to obtain the crude product. (1R, 2R, 5R)-2-Acetyl-5-methyl cyclohexanol and (1R, 2R, 5R)-2-Acetyl-5-methyl cyclohexanyl formate were obtained in 44% and 34% yield respectively after purification by silica gel column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06787671B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-810915b0e2bf4c31a80cb453c83aebd4 |
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| Source note | uspto-grants-2004_09 |
|---|