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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1985154생성일: 2026년 10월 25일

Sodium hydride → 2-Butoxy-3-(4-{2-(1-(3-methoxy-benzyl)-3-methyl-2-oxo-imidazolidin-4-yl]-ethoxy}-phenyl)-2-methyl-propionic acid ethyl ester

https://huagongshe.com/reaction/1985154

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물3-Methoxybenzyl bromideHCID 4067207—
반응물2-Butoxy-2-methyl-3-{4-[2-(3-methyl-2-oxo-imidazolidin-4-yl)-ethoxy]-phenyl}-propionic acid ethyl esterHCID 68867508—
촉매Tetrabutylammonium IodideHCID 67553—
용매Ethyl AcetateHCID 8857—
생성물2-Butoxy-3-(4-{2-(1-(3-methoxy-benzyl)-3-methyl-2-oxo-imidazolidin-4-yl]-ethoxy}-phenyl)-2-methyl-propionic acid ethyl esterHCID 68870062—

반응 단계

3-Methoxybenzyl bromide (0.024 mL, 0.170 mmol, d=1.436) and tetrabutyl ammonium iodide (catalytic amount) are added to a 0° C. suspension of 2-butoxy-2-methyl-3-{4-[2-(3-methyl-2-oxo-imidazolidin-4-yl)-ethoxy]-phenyl}-propionic acid ethyl ester (0.046 g, 0.114 mmol) and sodium hydride (0.011 g, 0.28 mmol, 60% suspension on mineral oil), pre-stirred for 1 h at ambient temperature. The reaction mixture is stirred at ambient temperature 48 h, diluted with ethyl acetate, and washed with 1N HCl and water. The organic layer is dried, concentrated, and used in the next step. MS [EI+] 527 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07544812B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-df5fea484bf74b7da62cb1e7904ae09f
출처 메모uspto-grants-2009_06