Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 67424113 | HCID 67424113 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 67423695 | HCID 67423695 | — |
Reaction Steps
Jones reagent (2 ml) was added dropwise to a stirred solution of the tetrol 7 (0.19 g, 0.45 mmol) in acetone (25 ml) at 0° C. and the mixture was stirred at room temperature for 1 h. Methanol (8 ml) was then added and the oxidized product was extracted with EtOAc (2×50 ml). The combined organic layers were dried over anhydrous sodium sulphate and evaporated to dryness under reduced pressure. The residue was dissolved in MeOH (80 ml), pTSA was added and the mixture was stirred at room temperature for 2 h. The solvent was evaporated under reduce pressure, the residue was dissolved in CHCl3 (50 ml), washed with a saturated aqueous solution of sodium bicarbonate (2×50 ml), water (50 ml) and brine (50 ml). The organic layer was dried over anhydrous sodium sulfate and evaporated to dryness. The residue was purified by flash chromatography using from 20 to 30% EtOAc in petroleum ether to afford the methyl ester 8 (0.115 g, 0.26 mmo, 58%1) as whitish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999964B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-fb828c0c672e45be9e316dba1aae6ffd |
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| Source note | uspto-grants-2015_04 |
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