HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-(2-hydroxymethylphenyl)-2-methoxyimino-N-methylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | 2-[2-{(1-ethoxyethyl)oxymethyl}phenyl]-2-methoxyimino-N-methylacetamide | HCID 53674405 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-(2-hydroxymethylphenyl)-2-methoxyimino-N-methylacetamide | HCID 54472560 | 90% |
Reaction Steps
Methanol (4 ml) and pyridinium p-toluenesulfonate (0.04 g, 0.00017 mol) were added to an E/Z mixture of 2-[2-{(1-ethoxyethyl)oxymethyl}phenyl]-2-methoxyimino-N-methylacetamide (0.50 g, 0.0017 mol), and the mixture was stirred under reflux for 2 hours. After completion of the reaction, half-saturated brine (100 ml) was added, and the mixture was extracted with dichloromethane (50 ml) twice. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (ethyl acetate/n-hexane) to obtain 2-(2-hydroxymethylphenyl)-2-methoxyimino-N-methylacetamide (0.34 g, Yield: 90.0%, E/Z=96/4) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05856573 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-125ffc03e32f4c31badab379434a35ee |
| Source note | uspto-grants-1999_01 |