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HRID 1284481생성일: 2026년 10월 26일

p-Toluenesulfonic acid monohydrate → 2-(Chloromethyl)-1-phenyl-1H-benzimidazole

https://huagongshe.com/reaction/1284481

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물N-(2-Anilinophenyl)-2-chloroacetamideHCID 14819969—
용매BenzeneHCID 241—
용매Sodium BicarbonateHCID 516892—
생성물2-(Chloromethyl)-1-phenyl-1H-benzimidazoleHCID 2025189636.5%

반응 단계

A solution of 2-chloro-N-(2-anilinophenyl)acetamide (10 g) and p-toluenesulfonic acid monohydrate (4.5 g) in benzene (250 ml) was refluxed for 1.5 hours under an azeotropic dehydration. After being cooled to ambient temperature, the reaction mixture was diluted with an aqueous sodium bicarbonate solution and extracted with ethyl acetate three times. The combined organic layer was washed successively with water and brine, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residual oil was purified by column chromatography on silica gel (100 g) with dichloromethane as an eluent to afford 2-chloromethyl-1-phenyl-1H-benzimidazole (3.4 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04563455
출처 데이터셋uspto-grants-1986_01
ORD IDord-5720073835484745bf2c062210db3bc8
출처 메모uspto-grants-1986_01