Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Potassium selenocyanate | HCID 76960 | — |
| Reactant | Mupirocin | HCID 446596 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 88784357 | HCID 88784357 | — |
| Solvent | 2,2-Dimethoxypropane | HCID 6495 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Pseudomonic acid C | HCID 10413058 | 45% |
Reaction Steps
Pseudomonic acid A (500 mgs) was dissolved in 2,2-dimethyoxypropane (50 ml) and treated with p-toluene sulphonic acid (few crystals). After 1 hour the solution was diluted with ethyl acetate, washed with brine and dried (MgSO4). The solution was evaporated in vacuo and the residue redissolved in water-methanol (1:1, 20 ml) and potassium bicarbonate (100 mgs, 1 eq) added. The solvents were removed in vacuo and potassium selenocyanate (432 mgs, 3 eq) and iso-hexylalcohol-water (9:1, 15 ml) added and reaction refluxed for 4 days. After filtering, the reaction mixture was diluted with ethyl acetate (20 ml) and extracted with aqueous sodium bicarbonate (3×20 ml). The aqueous extracts were combined and acidified with acetic acid under a layer of ethylacetate (20 ml). After stirring for ca. 1 hour the organic layer was separated and aqueous layer further extracted with ethylacetate (3×20 ml). The combined extracts were washed with brine, dried (MgSO4) and evaporated to an oil. Chromatography of the oil on silica (5 g) gave pure pseudomonic acid C (215 mgs, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04205002 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-8ae04c4f3e4047e181ce7d32a2af112f |
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| Source note | uspto-grants-1980_05 |
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