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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 514985생성일: 2026년 10월 24일

Methyl iodide → N-(2-Methoxy-5-nitro-phenyl)-N-methyl-propionamide

https://huagongshe.com/ko/reaction/514985

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물N-(2-methoxy-5-nitrophenyl)propanamideHCID 2176144—
용매TetrahydrofuranHCID 8028—
생성물N-(2-Methoxy-5-nitro-phenyl)-N-methyl-propionamideHCID 5916787795%

반응 조건

온도0 °C

반응 단계

To a stirred solution of 11.2 g (50.0 mmol) of (2) in 150 mL of anhydrous THF at 0° C. under the nitrogen, was added 3.0 g (75 mmol) of NaH (60% in oil). The suspension was stirred for 0.5 h at 0° C. and 10 mL (150 mmol) of iodomethane was added at 0° C. After the mixture warmed to room temperature and stirred for 3 h, the reaction was quenched by ice brine and extracted with EtOAc (200 mL). The organic phase was washed with brine, dried (Na2SO4), filtered, evaporated in vacuo and the solid was washed with hexane/EtOAc (9:1) to give pure product N-(2-Methoxy-5-nitro-phenyl)-N-methyl-propionamide (3) as a light yellow solid (11.3 g, 95% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09108933B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-4e379a2101e1400886bcbe72c6742a30
출처 메모uspto-grants-2015_08