HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756741Generated: October 24, 2026
Hydroxylamine, sulfate (1:1) → (E)-2-(Hydroxyimino)-N-methyl-2-(2-phenoxyphenyl)acetamide
https://huagongshe.com/en/reaction/1756741
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxylamine, sulfate (1:1) | HCID 159255 | — |
| Reactant | N-methyl-2-(2-phenoxyphenyl)-2-oxoacetamide | HCID 11780091 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (E)-2-(Hydroxyimino)-N-methyl-2-(2-phenoxyphenyl)acetamide | HCID 9816878 | 95.6% |
Reaction Steps
N-Methyl-2-(2-phenoxyphenyl)-2-oxoacetamide (2.55 g, 10 mmol) was dissolved in methyl alcohol (10 ml). Hydroxylamine sulfate (0.99 g, 12 mmol) was added, followed by heating under reflux for 3 hours. After completion of the reaction, methyl alcohol was evaporated under reduced pressure. Toluene (10 ml) and conc. hydrochloric acid (1.04 g) were added to the resulting residue (E/Z=41/59), and the mixture was stirred at room temperature for 20.5 hours. After completion of the reaction, water (300 ml) was added. The mixture was extracted with ethyl acetate (300 ml), washed with brine twice, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give (E)-N-methyl-2-(2-phenoxyphenyl)-2-hydroxyiminoacetamide (2.58 g, Yield: 95.6%, E/Z=96/4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05442063 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-7c9cf26173fc4b8faa042d219230fcd1 |
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| Source note | uspto-grants-1995_08 |
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