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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 751232생성일: 2026년 10월 25일

Methyl iodide → Methyl-[3-(4-trifluoromethoxy-phenyl)-prop-2-ynyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/751232

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물[3-(4-Trifluoromethoxy-phenyl)-prop-2-ynyl]-carbamic acid tert-butyl esterHCID 68823297—
용매DimethylformamideHCID 6228—
생성물Methyl-[3-(4-trifluoromethoxy-phenyl)-prop-2-ynyl]-carbamic acid tert-butyl esterHCID 6882445450%

반응 단계

[3-(4-Trifluoromethoxy-phenyl)-prop-2-ynyl]-carbamic acid tert-butyl ester (500 mg, 1.6 mmol) was added to an ice cold solution of iodomethane (100 μl, 1.7 mmol) and sodium hydride (73 mg, 1.7 mmol; 55% suspension in mineral oil) in DMF (5 ml). The reaction mixture was stirred for 5 h at ambient temperature, cooled to 0° C. and carefully quenched with saturated aqueous ammonium chloride solution. Ice water/ethyl acetate 1/1 were added, the layers were separated and the aqueous layer was extracted two times with ethyl acetate. The combined extracts were washed with brine and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by flash chromatography (silica gel, heptane/AcOEt) to give 258 mg (0.8 mmol, 49%) of the title compound as yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07405236B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-056b1c4f1bfd4bec8b704fdc0d0f432b
출처 메모uspto-grants-2008_07