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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54015Erstellt: 23. Oktober 2026

Water → 2,3-Dichloro-N-methylmaleimide

https://huagongshe.com/de/reaction/54015

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktDichloromaleic anhydrideHCID 70728—
EduktSodium ethoxideHCID 2723922—
EduktMethylamine hydrochlorideHCID 6364545—
LösungsmittelAcetic AcidHCID 176—
Produkt2,3-Dichloro-N-methylmaleimideHCID 1429364%

Reaktionsbedingungen

Temperatur25 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05621098
Quelldatensatzuspto-grants-1997_04
ORD IDord-852005cb9cfa4fc4bb7984493eefa91f
Quellennotizuspto-grants-1997_04