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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 511877생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/511877

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 (500 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 번호US09101614B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-c4b5c490692b4e868d568661cde3fb07
출처 메모uspto-grants-2015_08