HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-[2-(3,5-dichloropyridin-2-yl)-1-methyl-2-oxoethyl)phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Reactant | 2-Bromo-1-(3,5-dichloropyridin-2-yl)-1-propanone | HCID 118071562 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[2-(3,5-dichloropyridin-2-yl)-1-methyl-2-oxoethyl)phthalimide | HCID 118071579 | 32.9% |
Reaction Steps
To 5.00 g of 2-bromo-1-(3,5-dichloropyridin-2-yl)-1-propanone in 20 ml of N,N-dimethylformamide, 3.27 g of potassium phthalimide was added, and the mixture was stirred at room temperature for 2 hours. After completion of the reaction, the reaction mixture was mixed with 50 ml of water and extracted with ethyl acetate (50 ml×2), and the resulting organic layers were combined, washed with water (30 ml×1) and dried over saturated aqueous sodium chloride and then anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to obtain 2.02 g of the desired crude product as brown crystals. The crystals were 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-9dd1417c96a740a0a0cfacf3811df5ce |
| Source note | uspto-grants-2016_09 |