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HRID 477421Erstellt: 24. Oktober 2026

Nitrophenylgalactosides → (2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal

https://huagongshe.com/de/reaction/477421

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrophenylgalactosidesHCID 96647—
EduktSodium BicarbonateHCID 516892—
Produkt(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 3037556—

Reaktionsbedingungen

Temperatur37 °C

Reaktionsschritte

To a solution containing 30.12 g (100 mmol) o-nitrophenyl-β-D-galactoside in 1000 ml distilled water buffered at pH 6.8 with 0.5M phosphate buffer and maintained at 37° C. is added 10 mg of monoclonal antibodies prepared according to Example 6. The reaction mixture is gently agitated for 2.0 hours. The monoclonal antibodies are then recovered from the reaction mixture by ultrafiltration. The filtrate is then cooled to 10° C. and treated with 9.2 g (110 mmol) sodium bicarbonate. The D-galactose is recovered by extracting the filtrate with three 100 ml portions of diethyl ether. The ether portions are combined, washed once with 1.0N sodium bicarbonate, dried over magnesium sulfate, filtered and concentrated under reduced pressure to yield D-galactose. The aqueous portion is then combined with the sodium bicarbonate wash and acidified to pH 3 by the addition of 5N hydrochloric acid. The acidified aqueous portion is then extracted three times with ether. The etheral extracts are combined, dried over magnesium sulfate, filtered and concentrated at reduced pressure to yield o-nitrophenol. The o-nitrophenol and D-galactose may be further purified by HPLC or by recrystallization.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04888281
Quelldatensatzuspto-grants-1989_12
ORD IDord-ef615e3efaa140f0a2da634a16cb0614
Quellennotizuspto-grants-1989_12