HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55973Generated: October 29, 2026
Water → N-[2-(2,4-dichlorophenyl)-2-(methoxyimino)ethyl]phthalimide
https://huagongshe.com/reaction/55973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Reactant | 2-bromo-1-(2,4-dichlorophenyl)ethanone-O-methyloxime | HCID 118071616 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[2-(2,4-dichlorophenyl)-2-(methoxyimino)ethyl]phthalimide | HCID 118071602 | 79.1% |
Reaction Steps
To 2.17 g of 2-bromo-1-(2,4-dichlorophenyl)ethanone-O-methyloxime in 20 ml of N,N-dimethylformamide, 3.03 g of potassium phthalimide and 1.61 g of potassium carbonate were added, and the mixture was stirred at room temperature for 18 hours. After completion of the reaction, the reaction mixture was mixed with 40 ml of water and extracted with ethyl acetate (50 ml×1), the resulting organic layer was washed with water (20 ml×1) and then dried over saturated aqueous sodium chloride and then anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography using ethyl acetate-hexane (with a gradient of from 1:9 to 3:7) as the eluent to obtain 2.10 g of the desired product as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434684B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-c7e38a2a4cfe4577b970b6e0f7a09925 |
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| Source note | uspto-grants-2016_09 |
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