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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 263893생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/263893

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 stirred until H2 evolution has ceased and a clear solution was obtained (20 min.). (2-Acetoxyethoxy) methyl bromide (0.68 g, 10.66 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. Na2SO4) 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, 2H, C-1'), 4.143.92 (m, 4H, C-3' and C-4'), 1.83 (s, 3H, Ac). Anal. Calcd. for C12H9N2Cl5O3 : 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 번호US05646125
출처 데이터셋uspto-grants-1997_07
ORD IDord-999f1fb3e4fe4b368a89d1f265e38c7e
출처 메모uspto-grants-1997_07