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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54874생성일: 2026년 10월 24일

Water → 3-(4-Butylphenyl)-5-(4-methoxyphenyl)-2-oxazolidinone

https://huagongshe.com/ko/reaction/54874

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-(4-Methoxyphenyl)oxiraneHCID 98048—
반응물Lithium ChlorideHCID 433294—
반응물4-Butylphenyl isocyanateHCID 2796313—
용매DimethylformamideHCID 6228—
생성물3-(4-Butylphenyl)-5-(4-methoxyphenyl)-2-oxazolidinoneHCID 1995670214.5%

반응 단계

In a 20 ml-three necked flask, 0.013 g of lithium chloride and 3.8 ml of DMF were placed. To the mixture, a solution of 1.09 g (6.22 mM) of 4-butylphenyl isocyanate and 6.20 mM of optically active 4-methoxystyrene oxide in 1.3 ml of DMF was added dropwise in 12 minutes under refluxing and stirring in nitrogen atmosphere, followed by refluxing for 50 minutes under stirring. After the reaction, the reaction mixture was left standing for cooling, then poured into water, and subjected to extraction with ethyl acetate. The organic layer was washed with water, dried with anhydrous sodium sulfate and evaporated under reduced pressure to obtain a residue The residue was purified by silica gel column chromatography (eluent: toluene/ethyl acetate=10/1) and recrystallized from methanol to obtain 0.29 g of optically active 3-(4-butylphenyl)-5-(4-methoxyphenyl)-2-oxazolidinone (Yield: 14.5%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624600
출처 데이터셋uspto-grants-1997_04
ORD IDord-911e781ae40e4f81bc059adeb5bc3892
출처 메모uspto-grants-1997_04