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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55440생성일: 2026년 10월 23일

Water → 2,3-Dichloro-N-methylmaleimide

https://huagongshe.com/ko/reaction/55440

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Dichloromaleic anhydrideHCID 70728—
반응물Sodium ethoxideHCID 2723922—
반응물Methylamine hydrochlorideHCID 6364545—
용매Acetic AcidHCID 176—
생성물2,3-Dichloro-N-methylmaleimideHCID 1429364%

반응 조건

온도25 °C

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624949
출처 데이터셋uspto-grants-1997_04
ORD IDord-99833c5bcc6344e491e257e1a04e0a76
출처 메모uspto-grants-1997_04