HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → N-Methyl-3-[4-(4-nitrobenzyl)-2,5-dioxoimidazolidinylmethyl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-[(4-Nitrophenyl)methyl]imidazolidine-2,4-dione | HCID 10466579 | — |
| Reactant | 3-(chloromethyl)-N-methylbenzamide | HCID 22660208 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Methyl-3-[4-(4-nitrobenzyl)-2,5-dioxoimidazolidinylmethyl]benzamide | HCID 10068456 | 69.2% |
Reaction Steps
The product from step (a) (4.0 g), the product from step (b) (3.3 g) and anhy. K2CO3 (2.55 g) were taken up in DMF (25 ml) and stirred at room temperature for 60 hours. The mixture was poured with vigorous stirring into ice-water (175 ml) to give an oily precipitate. Ethyl acetate was added and stirring continued for 1 hour to solidify the precipitate. The latter was filtered off, washed with water, ethyl acetate and ether, and dried to give the desired product as a peach-coloured solid (4.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05225431 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-492dce69b7e9401193ac8693905e0858 |
| Source note | uspto-grants-1993_07 |