HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 1-(2-Bromoethyl)pyrrolidine-2,5-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Product | 1-(2-Bromoethyl)pyrrolidine-2,5-dione | HCID 13561395 | — |
Reaction Steps
To a mixture of dihydro-furan-2,5-dione (396 mg, 4.00 mmol) and 1,2-dibromo-ethane (1.50 g, 8.00 mmol) in CH3CN (20 ml) was added K2CO3 (829 mg, 6.00 mmol) at room temperature. The mixture was stirred at reflux overnight and the solvent was evaporated. The mixture was diluted with EtOAc (150 mL), washed with water, sat. Na2CO3aq., brine, and dried over MgSO4. The solvent was evaporated to give 1-(2-bromo-ethyl)-pyrrolidine-2,5-dione that was used for next step without further purification (580 mg, 70.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07674797B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-8ff54b2571a54a0fbec704ab580d56dd |
| Source note | uspto-grants-2010_03 |