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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395640Generated: October 30, 2026

p-Toluenesulfonic acid → Pseudomonic acid C

https://huagongshe.com/reaction/1395640

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantPotassium selenocyanateHCID 76960—
ReactantMupirocinHCID 446596—
ReactantPotassium BicarbonateHCID 516893—
ReactantHCID 88784357HCID 88784357—
Solvent2,2-DimethoxypropaneHCID 6495—
SolventEthyl AcetateHCID 8857—
ProductPseudomonic acid CHCID 1041305845%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04205002
Source datasetuspto-grants-1980_05
ORD IDord-8ae04c4f3e4047e181ce7d32a2af112f
Source noteuspto-grants-1980_05