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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2273279생성일: 2026년 10월 26일

Iodine → 2-(5,6-Dichloro-1H-benzoimidazol-2-yl)-1,1,1-trifluoro-cis-pent-3-en-2-ol

https://huagongshe.com/reaction/2273279

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물cis-1-Bromo-1-propeneHCID 643834—
반응물MagnesiumHCID 5462224—
반응물1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanoneHCID 11594370—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물2-(5,6-Dichloro-1H-benzoimidazol-2-yl)-1,1,1-trifluoro-cis-pent-3-en-2-olHCID 44443104—

반응 단계

To 1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone (510 mg) in THF (5 mL) at 0° C. was added Grignard reagent, which was freshly prepared from cis-1-bromo-1-propene (1.07 mL), a small iodine flake, and magnesium powder (306 mg) in THF (5 mL). The resulting mixture was then stirred at room temperature for 3 hr. The reaction was quenched with NH4Cl (sat. aq), filtered through a pad of Celite®, rinsed with EtOAc, the layers were separated, the aqueous layer extracted with EtOAc, dried over Na2SO4, filtered, and concentrated to yield a residue. The residue was purified by flash chromatography with Biotage 40s+ column and elution with 10%-40% EtOAc/hexanes to yield a yellow solid. The yellow solid was dissolved in a minimal amount of CH2Cl2 and triturated with hexanes to yield the title compound as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09120830B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-e36d347950b14ba4a854efa5c9ae1fb3
출처 메모uspto-grants-2015_09