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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 215703Erstellt: 26. Oktober 2026

Phosphate → 2-(2-methyl-phenyl)-N-methyl-2-hydroxy-acetamide

https://huagongshe.com/reaction/215703

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphateHCID 1061—
EduktNADPHHCID 5884—
EduktAmpicillinHCID 6249—
Eduktisopropyl beta-D-thiogalactopyranosideHCID 656894—
EduktN-methyl-2-(2-methylphenyl)-2-oxoacetamideHCID 15239356—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(2-methyl-phenyl)-N-methyl-2-hydroxy-acetamideHCID 66936442—

Reaktionsschritte

Using the plasmid pTrcGSRxc, E. coli HB101 was transformed. The resulting transformant was inoculated in a sterilized LB medium (100 ml) containing 0.1 mM of IPTG and 50 μg/ml of ampicillin, and was shaking-cultured (37° C., 15 hours). The resulting culture was centrifuged to obtain 0.1 g of wet bacterial cells. To a reaction tube were added 1.5 mg of 2-(2-methyl-phenyl)-N-methyl-2-oxo-acetamide, 0.1 g of the wet bacterial cells, 10 mg of NADPH, and 1.5 ml of a 100 mM phosphate buffer solution (pH 7), and these were reacted at a stirring rate of 1000 rpm at 30° C. for 20 hours. After the completion of the reaction, 5 ml of ethyl acetate was added to the reaction solution, and this was centrifuged (1000×g, 5 minutes) to recover an organic layer. The organic layer was distilled off to obtain oily 2-(2-methyl-phenyl)-N-methyl-2-hydroxy-acetamide. Content analysis by liquid chromatography under the following condition showed that the conversion rate was 87.2%. 1H-NMR analysis result of the resulting 2-(2-methyl-phenyl)-N-methyl-2-hydroxy-acetamide is shown below.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08192967B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-549572804a70462485547e6e2184e2a3
Quellennotizuspto-grants-2012_06