HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074339Generated: October 31, 2026
Ammonia → Ethyl 2-carbamoyl-2-(cyclopropyloxyimino)acetate
https://huagongshe.com/reaction/1074339
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl hydrogen alpha-(cyclopropyloxyimino)malonate | HCID 54136521 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-carbamoyl-2-(cyclopropyloxyimino)acetate | HCID 54332569 | — |
Reaction Steps
An activated acid, prepared from ethyl hydrogen α-(cyclopropyloxyimino)malonate (syn isomer)(19.78 g), phosphorus oxychloride (11.9 ml) and N,N-dimethylformamide (9.91 ml) by a conventional manner, was added to a saturated ammonia solution in tetrahydrofuran at -30° C. The mixture was gently warmed to ambient temperature. The mixture was poured into a mixture of ethyl acetate (1 l) and ice-water (1 l) and adjusted to pH 7 with saturated aqueous solution of sodium bicarbonate. The organic layer was separated washed with saturated aqueous solution of sodium chloride, dried over magnesium sulfate and concentrated in vacuo. The residue was subjected to column chromatography on silica gel (200 g) using chloroform as an eluent to give ethyl 2-carbamoyl-2-(cyclopropyloxyimino)acetate (syn isomer) as a crystal (10.51 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04973699 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-c55138e435294b2bb1e55d81df14f102 |
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| Source note | uspto-grants-1990_11 |
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