HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-amino-1-(3,5-dichloropyridin-2-yl)ethanone-O-propyloxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | N-[2-(3,5-dichloropyridin-2-yl)-2-(propoxyimino)ethyl]phthalimide | HCID 118071539 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-amino-1-(3,5-dichloropyridin-2-yl)ethanone-O-propyloxime | HCID 118071509 | 96.1% |
Reaction Steps
To 235 mg of N-[2-(3,5-dichloropyridin-2-yl)-2-(propoxyimino)ethyl]phthalimide in 5 ml of ethanol, 90 mg of hydrazine monohydrate was added and refluxed with heating for 3 hours with stirring. After completion of the reaction, the reaction mixture was allowed to cool to room temperature, mixed with 20 ml of water and extracted with ethyl acetate (35 ml×2). The resulting organic layers were combined, washed with water (20 ml×1) and dried over saturated aqueous sodium chloride and then anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to obtain 151 mg of the desired crude product as a brown oil. The oil was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434684B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-d89d82bde57a4f2da458ae44b5d6ec04 |
| Source note | uspto-grants-2016_09 |