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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707269Generated: October 26, 2026

Propanoic acid, 3-iodo- → Rhizoxin 3-iodopropionate

https://huagongshe.com/reaction/1707269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanoic acid, 3-iodo-HCID 8856—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-PyrrolidinopyridineHCID 75567—
ReactantRhizoxinHCID 6437358—
SolventTolueneHCID 1140—
ProductRhizoxin 3-iodopropionateHCID 8674816780.7%

Reaction Steps

1.03 g of DCC and a catalytic amount of 4-pyrrolidinopyridine were added to a solution of 1.25 g of rhizoxin and 1.20 g of 3-iodopropionic acid in toluene, and the resulting mixture was stirred at room temperature for 2 hours. At the end of this time, the reaction mixture was treated in the same manner as described in Example 1, to give 1.33 g of rhizoxin 3-iodopropionate. The whole of this ester was immediately dissolved in 20 ml of acetonitrile, and 0.92 g of the silver salt of methylmercaptan prepared at the time of use was added. The resulting mixture was stirred at room temperature for 8 hours, after which the precipitate was filtered off. The solvent was then removed by distillation under reduced pressure, and ethyl acetate was added to the residue. The resulting mixture was washed with a 5% w/v aqueous solution of sodium bicarbonate and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure, and the residue was purified by silica gel column chromatography, using a 1:1 by volume mixture of cyclohexane and ethyl acetate as eluent, to give 970 mg of the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05352689
Source datasetuspto-grants-1994_10
ORD IDord-26327fe3a74a4918adb457f31a517390
Source noteuspto-grants-1994_10