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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242371생성일: 2026년 10월 25일

Ammonium Chloride → 1-[1-Ethoxymethyl-4-(triethylsilyloxymethyl)-1H-imidazol-2-yl]ethanone

https://huagongshe.com/reaction/242371

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물N-Methoxy-N-methylacetamideHCID 537505—
반응물1-Ethoxymethyl-4-(triethylsilyloxymethyl)-1H-imidazoleHCID 71087126—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-[1-Ethoxymethyl-4-(triethylsilyloxymethyl)-1H-imidazol-2-yl]ethanoneHCID 71087197—

반응 조건

온도-78 °C

반응 단계

The compound (665 mg) obtained in (3) was dissolved in THF (20 mL), and cooled to −78° C. while stirring under an argon atmosphere. To the present solution was added dropwise n-butyl lithium (2.69 M hexane solution, 1.50 mL) slowly using a syringe, followed by stirring at the same temperature for 30 minutes. Then, N-methoxy-N-methylacetamide (0.50 mL) was added using a syringe, and stirring was continued for 17 hours while the temperature was raised to room temperature. A saturated aqueous ammonium chloride solution was added to the reaction solution to terminate the reaction, followed by extraction with ethyl acetate. The combined extract was washed with saturated brine, dried over anhydrous sodium sulfate, and subsequently the solvent was distilled off under reduced pressure. The resulting residue was purified by flash chromatography (ethyl acetate/hexane=5%→30%) using silica gel column (product name: SNAP Cartridge KP-Sil 50 g, manufactured by Biotage, Ltd.) to afford the title compound (520 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653126B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-73cc6da7e7a2401c83c4203824121362
출처 메모uspto-grants-2014_02