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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 65439Erstellt: 23. Oktober 2026

Potassium Phosphate, Dibasic → 3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone

https://huagongshe.com/de/reaction/65439

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, DibasicHCID 24450—
EduktSodium PersulfateHCID 62655—
Edukt1-p-methoxybenzyl-3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinoneHCID 18604772—
KatalysatorFerrous sulfate heptahydrateHCID 62662—
KatalysatorCupric acetate monohydrateHCID 165397—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinoneHCID 18604774—

Reaktionsschritte

A solution of 68.3 mg (0.2 mmol) of 1-p-methoxybenzyl-3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone in 4 ml of acetonitrile is added to a solution of 428 mg (1.8 mmol) of sodium peroxydisulphate, 174 mg (1 mmol) of dipotassium hydrogen phosphate, 1 mg of iron(II) sulphate heptahydrate and 2 mg of copper(II) acetate hydrate in 4 ml of water. The mixture is stirred for 2 hours under an argon atmosphere at a bath temperature of 65°. The resulting mixture is then concentrated to half its volume under reduced pressure and extracted with ethyl acetate. The extract is triturated with methylene chloride and ether and the pure title compound is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04614614
Quelldatensatzuspto-grants-1986_09
ORD IDord-139ed6457cd64e2e9fcb010d4805aeea
Quellennotizuspto-grants-1986_09