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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1857698생성일: 2026년 10월 26일

Methyl iodide → 5-(3,5-dichlorophenylthio)-1-methyl-4-isopropyl-2-(p-methoxybenzyloxymethyl)-1H-imidazole

https://huagongshe.com/reaction/1857698

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
반응물HCID 178491401HCID 178491401—
용매DimethylformamideHCID 6228—
생성물5-(3,5-dichlorophenylthio)-1-methyl-4-isopropyl-2-(p-methoxybenzyloxymethyl)-1H-imidazoleHCID 2213054815%

반응 단계

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 magnisium 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06147097
출처 데이터셋uspto-grants-2000_11
ORD IDord-c1a48a06949642dba22d5e1ca03eb63d
출처 메모uspto-grants-2000_11