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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 723672생성일: 2026년 10월 26일

Methyl iodide → 4-Fluoro-N-methyl-N-[2-(5-methyl-furan-2-yl)-ethyl]-benzamide

https://huagongshe.com/reaction/723672

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물4-Fluoro-N-[2-(5-methyl-2-furanyl)ethyl]benzamideHCID 21874846—
용매TetrahydrofuranHCID 8028—
생성물4-Fluoro-N-methyl-N-[2-(5-methyl-furan-2-yl)-ethyl]-benzamideHCID 2187496284%

반응 단계

NaH (60% dispersion in oil, 65 mg, 1.63 mmol) was added portionwise to a solution of 4-fluoro-N-[2-(5-methyl-2-furanyl)ethyl]benzamide (269 mg, 1.09 mmol, 237A) in THF (5 mL). After gas evolution ceased, iodomethane (0.14 mL, 2.18 mmol) was added drop-wise. Once HPLC analysis showed the reaction to be 50% complete, the mixture was concentrated under reduced pressure and resubjected to the above conditions. After all the starting material was consumed, H2O was added and the resulting mixture was extracted with EtOAc (2×5 mL). The combined organic layers were dried over Na2SO4 and concentrated under reduced pressure. Purification by flash chromatography on silica gel eluting with 20% acetone/CHCl3 gave 238 mg (84%) of compound 425A. HPLC: 98% at 2.94 min (retention time) (Phenomenex-prime S5-C18 column 4.6×50 mm eluting with 10–90% aqueous methanol over 4 minutes containing 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm). MS (ES): m/z [M+H]=262.38.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07141578B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-b3934f16316f48639f3ea9f7a704bd0a
출처 메모uspto-grants-2006_11