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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 274899Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/274899

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropanoic acid, 3-iodo-HCID 8856—
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt4-PyrrolidinopyridineHCID 75567—
EduktRhizoxinHCID 6437358—
LösungsmittelTolueneHCID 1140—
ProduktRhizoxin 3-iodopropionateHCID 8674816780,7%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05391564
Quelldatensatzuspto-grants-1995_02
ORD IDord-745364b5b29043b39a34a52823d2783a
Quellennotizuspto-grants-1995_02