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HRID 2379067作成日:2026年10月27日

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

https://huagongshe.com/reaction/2379067

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物2-(Bromomethoxy)ethyl acetateHCID 367656—
反応物2,4,5,6,7-pentachloro-1H-benzimidazoleHCID 23273974—
溶媒AcetonitrileHCID 6342—
生成物2,4,5,6,7-Pentachloro-1-(2-acetoxyethoxymethyl)benzimidazoleHCID 18697573—

反応手順

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, 2, H, C-1'), 4.143.92 (m, 4, H, C-3' and C-4'), 1.83 (s, 3 H, Ac). Anal. Calcd. for C12H9N2Cl5O3 : C,35.45; H, 2.23; N, 6.89. Found: C,35.57; H, 2.17; N, 16.91.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05360795
出典データセットuspto-grants-1994_11
ORD IDord-dd1825c301ad42ddadfe48af9e09e6c9
出典メモuspto-grants-1994_11