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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493895Generated: October 25, 2026

Nitrophenylgalactosides → 2-Nitrophenol

https://huagongshe.com/reaction/493895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrophenylgalactosidesHCID 96647—
Reactantaldehydo-D-XyloseHCID 644160—
ReactantGaxiloseHCID 3082054—
ReactantMercapto-ethanolHCID 4713212—
ReactantMagnesium ChlorideHCID 5360315—
ReactantMonopotassium phosphate dipotassium phosphateHCID 21889592—
SolventWaterHCID 962—
Product2-NitrophenolHCID 6947—

Reaction Conditions

Temperature100 °C

Reaction Steps

In order to synthesize 4-O-β-D-galactopyranosyl-D-xylose, 5 g of o-nitrophenyl β-D-galactopyranoside (Gal-ONP) and 25 g of D-xylose were dissolved in 330 ml of water buffered to a pH of 7 (0.05 M KH2PO4/K2HPO4, 1 mM MgCl2, 5 mM mercaptoethanol), 2 mg (640 u) of E. coli β-galactosidase enzyme were added and the solution thus obtained was subjected to incubation at 37° C. in an orbital stirrer until the Gal-ONP was practically consumed (approximately 2 hours). Following the methodology put forth in example 3, the reaction was stopped by heating at 100° C. for 10 minutes and the ortho-nitrophenol formed was extracted with ethyl acetate. The aqueous solution was concentrated up to an approximate volume of 50 ml, filtered through glass wool and passed through the active carbon/celite column.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07537909B2
Source datasetuspto-grants-2009_05
ORD IDord-7dc500de84b94e2e965eac6679d7d64a
Source noteuspto-grants-2009_05