HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2,6-dimethyl-N-(2-methoxyimino-prop-1-yl)-N-methoxyacetylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | 2,6-dimethyl-N-methoxyacetyl-N-acetonylaniline | HCID 13071323 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,6-dimethyl-N-(2-methoxyimino-prop-1-yl)-N-methoxyacetylaniline | HCID 54160569 | 94.3% |
Reaction Steps
20 g (0.08 mol) of 2,6-dimethyl-N-methoxyacetyl-N-acetonylaniline, 7.5 g (0.09 mol) of O-methyl-hydroxylamine hydrochloride and 9.1 g (0.09 mol) of triethylamine in 100 ml of ethanol were heated under reflux for 5 hours. After distilling off the solvent in vacuo, the residue was partitioned between water/methylene chloride. The organic phase was separated off, dried over sodium sulphate and concentrated. After adding petroleum ether, the residue crystallized. 21 g (94% of theory) of 2,6-dimethyl-N-(2-methoxyimino-prop-1-yl)-N-methoxyacetylaniline of melting point 56°-57° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04337268 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-e0d31e4f7f3d40dd8c90e5b93ad8b457 |
| Source note | uspto-grants-1982_06 |