Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
p-Toluenesulfonic acid monohydrate → 2-(Chloromethyl)-1-phenyl-1H-benzimidazole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 반응물 | N-(2-Anilinophenyl)-2-chloroacetamide | HCID 14819969 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Sodium Bicarbonate | HCID 516892 | — |
| 생성물 | 2-(Chloromethyl)-1-phenyl-1H-benzimidazole | HCID 20251896 | 36.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04563455 |
| 출처 데이터셋 | uspto-grants-1986_01 |
| ORD ID | ord-5720073835484745bf2c062210db3bc8 |
| 출처 메모 | uspto-grants-1986_01 |