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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64994Erstellt: 23. Oktober 2026

Phenylacetic Acid → 6-Aminopenicillanic acid

https://huagongshe.com/de/reaction/64994

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenylacetic AcidHCID 999—
EduktPenicillin GHCID 5904—
EduktSodium HydroxideHCID 14798—
Eduktp-Dimethylaminobenzaldehyde methanolHCID 20437094—
EduktPenicillin G PotassiumHCID 23664709—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelPhosphateHCID 1061—
Produkt6-Aminopenicillanic acidHCID 11082—

Reaktionsbedingungen

Temperatur28 °C

Reaktionsschritte

An amount of penicillin acylase enzyme, either free or immobilized on the carrier, sufficient to contain about 50 I.U. of activity, was suspended in 60 ml of 7.5-pH phosphate buffer. The mixture was maintained at 28° C. in a vessel connected to a pH controller which electrometrically determined the pH and metered in sufficient 0.8 N sodium hydroxide solution to maintain the pH at approximately 8.0. A solution containing 5 g of penicillin G potassium salt in phosphate buffer, also at 28° C., was added to the vessel, and the rate of formation of phenylacetic acid by the enzyme-catalyzed hydrolysis of the penicillin G was determined from the rate of addition of sodium hydroxide solution to maintain the pH. The liquid in the vessel was sampled upon addition of the penicillin G salt and after 10 and 30 minutes. These samples (0.5 ml) were immediately mixed with 3 ml of a solution of 1 ml of 0.05 M sodium hydroxide, 2 ml of 20% acetic acid and 0.5% (weight-volume) p-dimethylaminobenzaldehyde/methanol, and were allowed to stand for 10 minutes. The amount of 6-aminopenicillanic acid formed was determined by spectrophotometrically measuring the light absorption of the mixture at a wave length of 415 nm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04612288
Quelldatensatzuspto-grants-1986_09
ORD IDord-720609f0e522413ab8f16c30b91add24
Quellennotizuspto-grants-1986_09