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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 263534생성일: 2026년 10월 27일

Water → 1,9-Bis[4-[(3,5-dioxo-1,2,4-oxadiazolidin-2-yl)methyl]phenoxy]nonane

https://huagongshe.com/reaction/263534

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium HydroxideHCID 14798—
반응물ethyl N-carbonylcarbamateHCID 300166—
반응물1,9-Bis[4-(hydroxyaminomethyl)phenoxy]nonaneHCID 19038524—
반응물tetrahydrofuran N,N-dimethylformamideHCID 21974620—
생성물1,9-Bis[4-[(3,5-dioxo-1,2,4-oxadiazolidin-2-yl)methyl]phenoxy]nonaneHCID 19038457—

반응 단계

1,9-Bis[4-(hydroxyaminomethyl)phenoxy]nonane (1.07 g) was dissolved in 75 ml of tetrahydrofuran-dimethylformamide (4:1) and, in an atmosphere of argon and with ice-cooling, 0.75 ml of ethoxycarbonyl isocyanate was added dropwise to the solution. After 10 minutes of stirring, 1N sodium hydroxide aqueous solution was added dropwise to the reaction mixture with water-cooling, followed by 2 hours of stirring at room temperature. The solvent was evaporated under a reduced pressure, and the thus obtained residue was mixed with 1N hydrochloric acid and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated sodium chloride aqueous solution in that order and dried over anhydrous magnesium sulfate. Then, the solvent was evaporated under a reduced pressure. The resulting residue was subjected to silica gel column chromatography, and the thus obtained 0.78 g of crude product obtained from fractions of chloroform-methanol (40:1) elution was recrystallized from methanol to obtain 0.69 g of 1,9-bis[4-[(3,5-dioxo-1,2,4-oxadiazolidin-2-yl)methyl]phenoxy]nonane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05643931
출처 데이터셋uspto-grants-1997_07
ORD IDord-ac46ca30274b4a49b33f2170f1560a05
출처 메모uspto-grants-1997_07