HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888711Generated: November 1, 2026
Phosphate → 2-(2-methyl-phenyl)-N-methyl-2-hydroxy-acetamide
https://huagongshe.com/reaction/888711
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphate | HCID 1061 | — |
| Reactant | NADP nicotinamide-adenine-dinucleotide phosphate | HCID 5886 | — |
| Reactant | Ampicillin | HCID 6249 | — |
| Reactant | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| Reactant | isopropyl beta-D-thiogalactopyranoside | HCID 656894 | — |
| Reactant | N-methyl-2-(2-methylphenyl)-2-oxoacetamide | HCID 15239356 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(2-methyl-phenyl)-N-methyl-2-hydroxy-acetamide | HCID 66936442 | 74.2% |
Reaction Steps
Using the plasmid pTrcGSRs, 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 0.5 g of wet bacterial cells. To a reaction tube were added 30 mg of 2-(2-methyl-phenyl)-N-methyl-2-oxo-acetamide, 0.5 g of the wet bacterial cells, 30 mg of NADP+, 45 mg of glucose, and 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 24 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 22.5 mg of oily 2-(2-methyl-phenyl)-N-methyl-2-hydroxy-acetamide. 1H-NMR analysis result of the resulting 2-(2-methyl-phenyl)-N-methyl-2-hydroxy-acetamide is shown below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252563B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-4cf9e1c6dea8445593902a4f0fc42049 |
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| Source note | uspto-grants-2012_08 |
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