Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Dichloromaleic anhydride | HCID 70728 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Edukt | Methylamine hydrochloride | HCID 6364545 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 2,3-Dichloro-N-methylmaleimide | HCID 14293 | 64% |
Reaktionsschritte
Sodium ethoxide (3.56 g, 50 mmol) was added to a solution containing 2,3-dichloromaleic anhydride (5.56 g, 33.3 mmol) and methylamine hydrochloride (3.50 g, 55.0 mmol) in 40 mL of acetic acid. The mixture was stirred under a CaCl2 drying tube at 25° C. for 16 hours and then refluxed for 4 hours. The cooled mixture was poured into water (350 mL) and extracted with EtOAc (3×75 mL). The combined organic extracts were washed with 100 mL portions of saturated aqueous NaHCO3, water and brine and dried (MgSO4). The solvent was evaporated under reduced pressure. The residue was recrystallized from ethanol to give 3.82 g (64%) of 2,3-dichloro N-methylmaleimide as white crystals. Concentration of the mother liquor and chromatography of the residue by radial preparative layer chromatography (Chromatotron, Harrison Research), gave an additional 0.81 g of 2,3-dichloro N-methylmaleimide, raising the yield to 77%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05624949 |
|---|
| Quelldatensatz | uspto-grants-1997_04 |
|---|
| ORD ID | ord-99833c5bcc6344e491e257e1a04e0a76 |
|---|
| Quellennotiz | uspto-grants-1997_04 |
|---|