Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl oxoacetate | HCID 70211 | — |
| Reactant | N-methylhydroxylamine hydrochloride | HCID 77906 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86734657 | HCID 86734657 | — |
Reaction Steps
The above mixture of ethyl glyoxylate and acetic acid (11.34 g, containing 70 mmol aldehyde) is dissolved in methanol (110 ml), N-methylhydroxylamine hydrochloride (5.8 g) and sodium acetate trihydrate (10.9 g) are added and the mixture is stirred at room temperature for 24 hours. It is then concentrated in vacuo, diluted with water and extracted with dichloromethane. The dichloromethane solution is then washed with a dilute sodium bicarbonate solution and water, dried over anhydrous magnesium sulfate, evaporated and distilled to afford α-ethoxy-carbonyl-N-methyl nitrone as a colorless solid (5.0 g), boiling point 80°-85° C/0.4 mm of Hg., melting point 43°-49° C. This is a mixture of the syn- and anti-isomers on the basis of the nmr spectrum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04018774 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-65f28756623143b6a25d15b17258ba4c |
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| Source note | uspto-grants-1977_04 |
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