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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 232322생성일: 2026년 10월 26일

Water → 2-[4-(1H-imidazol-1-yl)phenoxy]-N-(phenylmethyl)ethanamine

https://huagongshe.com/reaction/232322

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물1-(p-Hydroxyphenyl)imidazoleHCID 82315—
반응물Benzenemethanamine, N-(2-chloroethyl)-, hydrochloride (1:1)HCID 13054189—
용매DimethylformamideHCID 6228—
용매Dichloromethane methanolHCID 21226129—
생성물2-[4-(1H-imidazol-1-yl)phenoxy]-N-(phenylmethyl)ethanamineHCID 14555625—

반응 단계

To a chilled suspension of 39.5 g (0.823 mol) 50% sodium hydride in 500 mL dimethylformamide add 37.32 g (0.233 mol) 4-(1H imidazol-1-yl)phenol. When the addition is complete, stir the reaction mixture at room temperature until gas evolution ceases. After this time, chill the reaction mixture below 0° C. and slowly add 60.22 g (0.292 mol) N-benzyl(2-chloro)ethylamine hydrochloride. When the addition is complete, heat the reaction mixture to 65° C. Follow the progress of the reaction by thin-layer chromatography on silica gel (methylene chloride:methanol) (9:1). At the completion of the reaction, add 20 mL water to the cooled mixture. Filter the slats and remove the solvents in vacuo to obtain an oil. Column chromatograph the oil on silica gel using methylene chloride+methanol (1+99→1+19) as eluent. Collect the appropriate fractions and remove the solvents to obtain the title compound as the free base. Dissolve the free base in excess methanolic HCl solution and remove the solvent in vacuo to provide the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04851526
출처 데이터셋uspto-grants-1989_07
ORD IDord-9ce88200164d4d8bb79a0337f4665721
출처 메모uspto-grants-1989_07