Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1415995생성일: 2026년 10월 25일
Methyl iodide → 5-(3,5-dichlorophenylthio)-1-methyl-4-isopropyl-2-(p-methoxybenzyloxymethyl)-1H-imidazole
https://huagongshe.com/reaction/1415995
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | HCID 178491401 | HCID 178491401 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 5-(3,5-dichlorophenylthio)-1-methyl-4-isopropyl-2-(p-methoxybenzyloxymethyl)-1H-imidazole | HCID 22130548 | 80.7% |
반응 단계
(5)In 25 ml of dry N,N-dimethylformamide was dissolved 11.0 g (25.1 mmol)of 5-(3,5-dichlorophenylthio)-4-isopropyl-2-(p-methoxybenzyloxymethyl)-1H-imidazole (16b), followed by addition of 5.2 g (38 mmol)of potassium carbonate powder. Then, 3.90 g (27.7 mmol)of methyl iodide was further added and the mixture was stirred at room temperature for 8 hours. This reaction mixture was concentrated under reduced pressure and the residue was diluted with water and extracted with diethyl ether. The organic layer was washed with water and dried over magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was fractionated by silica gel chromatography (ethyl acetate:methylene chloride=1:9). From the first fraction, 1.7 g (yield 15%)of the objective position isomer (17b')was obtained as oil. From the subsequent fraction, 9.14 g (yield 80%)of the objective 5-(3,5-dichlorophenylthio)-1-methyl-4-isopropyl-2-(p-methoxybenzyloxymethyl)-1H-imidazole (17b)was obtained. mp 79-80° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05910506 |
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| 출처 데이터셋 | uspto-grants-1999_06 |
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| ORD ID | ord-afec6b9e1c11450b9afb8aebc418a119 |
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| 출처 메모 | uspto-grants-1999_06 |
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