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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 724865생성일: 2026년 10월 25일

Sodium hydride → 2,4,5,6,7-Pentachloro-1-(2-acetoxyethoxymethyl)benzimidazole

https://huagongshe.com/reaction/724865

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-(Bromomethoxy)ethyl acetateHCID 367656—
반응물2,4,5,6,7-pentachloro-1H-benzimidazoleHCID 23273974—
용매AcetonitrileHCID 6342—
생성물2,4,5,6,7-Pentachloro-1-(2-acetoxyethoxymethyl)benzimidazoleHCID 18697573—

반응 단계

NaH (0.12 g, 3.0 mmole, 60% oil disperson) was added to a stirred suspension of 2,4,5,6,7-pentachlorobenzimidazole (14) (1.0 g, 3.4.mmole) in dry CH3CN (120 mL) under a N2 atmosphere. The solution was surfed until H2 evolution has ceased and a clear solution was obtained (20 min.). (2-Acetoxyethoxy) methyl bromide (0.68 g, 10.68 mmole) in CH3CN (34 mL) was then added dropwise. The reaction mixture was stirred for an additional 3 hr. The resulting mixture was concentrated under reduced pressure, diluted with H2O (50 mL), extracted with EtOAc (100 mL), washed with H2O (100 mL), dried (anhyd. Na2 SO4) and the solvent was removed under reduced pressure to yield an oil (165). The resulting oil was purified by flash column chromatography (2×24 cm) (230-400 mesh). Elution of the column with hexane:EtOAc (6:4, v/v) and evaporation of the appropriate fractions gave a solid which was recrystallized from MeOH to afford 1.39 g (72%) of 165: m.p. 119° C. 1H NMR (CDCl3): d 5.93 (s, 2 H, C-1'), 4.143.92 (m, 4 H, C-3' and C-4'), 1.83 (s, 3 H, Ac). Anal. Calcd. for C12 H9N2Cl5O3 : C,35.45; H, 2.23; N, 6.89. Found: C, 35.57; H, 2.17; N, 16.91.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05705490
출처 데이터셋uspto-grants-1998_01
ORD IDord-6b209c5345d14b74892590b23cfe8f09
출처 메모uspto-grants-1998_01