HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Methyl 3-imino-3-methoxy-2-ethoxyiminopropionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Phenolphthalein | HCID 4764 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl 2-cyano-2-ethoxyiminoacetate | HCID 53675257 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-imino-3-methoxy-2-ethoxyiminopropionate | HCID 54122709 | — |
Reaction Steps
To a solution of methyl 2-cyano-2-ethoxyiminoacetate (syn isomer) (4.7 g) in methanol (50 ml) was added 1 N methanolic solution (5 ml) of sodium methoxide under cooling in an ice-bath and stirring, which was continued for 20 minutes in an ice-bath and 15 minutes at room temperature. The mixture was neutralized to the end point of phenolphthalein with 1 N methanolic solution of acetic acid and evaporated. The residue was dissolved in methylene chloride (80 ml), washed with water, dried over magnesium sulfate and evaporated to give methyl 3-imino-3-methoxy-2-ethoxyiminopropionate (syn isomer) (4.8 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04407798 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-d0490670f8fa4ae5adf7b8a6a6770d0a |
| Source note | uspto-grants-1983_10 |