HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779719Generated: October 31, 2026
Hydroxylamine, sulfate (1:1) → (2E)-2-[2-[(2,5-dimethylphenoxy)methyl]phenyl]-2-hydroxyimino-N-methylacetamide
https://huagongshe.com/reaction/1779719
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxylamine, sulfate (1:1) | HCID 159255 | — |
| Reactant | 2-[2-(2,5-dimethylphenoxymethyl)phenyl]-N-methyl-2-oxoacetamide | HCID 11087792 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2E)-2-[2-[(2,5-dimethylphenoxy)methyl]phenyl]-2-hydroxyimino-N-methylacetamide | HCID 15790180 | 90.6% |
Reaction Steps
N-methyl-2-[2-(2,5-dimethylphenoxymethyl)phenyl]-2-oxoacetamide (11.89 g, 0.04 mol) was suspended in methanol (40 ml). Hydroxylamine sulfate (4.92 g, 0.06 mol) was added, and the mixture was refluxed for 8 hours. After completion of the reaction, methanol was evaporated under reduced pressure. The resulting residue (E/Z=46/54) was dissolved in methylene chloride (80 ml), conc. hydrochloric acid (20 ml) was added, and the mixture was stirred at room temperature for 15 hours. Water (50 ml) and toluene (80 ml) were added, and the mixture was stirred at room temperature for 5 minutes. Then the resulting crystals were separated by filtration, washed with water (50 ml) and toluene (50 ml) and dried to give (E)-N-methyl-2-[2-(2,5-dimethylphenoxymethyl)phenyl]-2-hydroxyiminoacetamide (11.32 g, Yield: 90.6%, E/Z=99/1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05627284 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-6b33f9706847465dbc276de1f94122fc |
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| Source note | uspto-grants-1997_05 |
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