Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 258859생성일: 2026년 10월 26일
Potassium Iodide → 1-{4-[4-(4-fluorobenzoyl)-1-piperidinyl]butyl}-1,3-dihydro-2H-benzimidazol-2-one
https://huagongshe.com/reaction/258859
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | p-Fluorophenyl 4-piperidyl ketone hydrochloride | HCID 3084438 | — |
| 반응물 | 1-(4-chlorobutyl)-1,3-dihydro-2H-benzimidazol-2-one | HCID 13360889 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Methyl Isobutyl Ketone | HCID 7909 | — |
| 생성물 | 1-{4-[4-(4-fluorobenzoyl)-1-piperidinyl]butyl}-1,3-dihydro-2H-benzimidazol-2-one | HCID 54155158 | 30% |
반응 단계
A mixture of 4 parts of 1-(4-chlorobutyl)-1,3-dihydro-2H-benzimidazol-2-one, 4 parts of (4-fluorophenyl) (4-piperidinyl) methanone hydrochloride, 10 parts of sodium carbonate, 0.2 parts of potassium iodide and 80 parts of 4-methyl-2-pentanone is stirred and refluxed overnight. After cooling, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The solid residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 10% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 4-methyl-2-pentanone, yielding 2 parts (30%) of 1-{4-[4-(4-fluorobenzoyl)-1-piperidinyl]butyl} -1,3-dihydro-2H-benzimidazol-2-one; mp. 176.5° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04035369 |
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| 출처 데이터셋 | uspto-grants-1977_07 |
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| ORD ID | ord-fc9d249e84de44eebf843f8c59c1d2ba |
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| 출처 메모 | uspto-grants-1977_07 |
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