HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Methyl 2-cyano-2-ethoxyiminoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Methyl 3-amino-2-(ethoxyimino)-3-oxopropanoate | HCID 53690437 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Methyl 2-cyano-2-ethoxyiminoacetate | HCID 53675257 | 90.4% |
Reaction Steps
To a solution of methyl 2-carbamoyl-2-ethoxyiminoacetate (syn isomer) (5.22 g) in pyridine (50 ml) was dropwise added trifluoroacetic anhydride (15.7 g) below 25° C. under cooling in an ice-bath and stirring, which was continued for 30 minutes. The reaction mixture was poured into water (200 ml), followed by an addition of diisopropyl ether (200 ml). The mixture was adjusted to pH 2 with 6 N hydrochloric acid (80 ml) at 15° to 20° C. and the organic layer was separated out, washed with water, dried over magnesium sulfate and evaporated to give methyl 2-cyano-2-ethoxyiminoacetate (syn isomer) (4.23 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-13b17d3aa9324f2faf70afbbe582d7d5 |
| Source note | uspto-grants-1983_10 |