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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219020생성일: 2026년 10월 25일

Phosphate → 5-(2,2-Dimethyl-4H-1,3-benzodioxin-6-yl)-3-{6-[2-{(3-nitrophenyl)-methoxy}ethoxy]hexyl}-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/219020

반응식

참여 물질

역할이름HCID투입량
반응물PhosphateHCID 1061—
반응물Sodium hydrideHCID 24758—
반응물(5R)-5-(2,2-Dimethyl-4H-1,3-benzodioxin-6-yl)-1,3-oxazolidin-2-oneHCID 10933894—
반응물1-[(2-[(6-Bromohexyl)oxy]ethoxy)methyl]-3-nitrobenzeneHCID 46833106—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물5-(2,2-Dimethyl-4H-1,3-benzodioxin-6-yl)-3-{6-[2-{(3-nitrophenyl)-methoxy}ethoxy]hexyl}-1,3-oxazolidin-2-oneHCID 75215614101.8%

반응 단계

A solution of (5R)-5-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-1,3-oxazolidin-2-one (4.40 g) in anhydrous DMF (75 ml) was treated under nitrogen at 0° with sodium hydride (60% dispersion in mineral oil, 1.04 g) and the mixture stirred for 40 min. A solution of 1-[(2-[(6-bromohexyl)oxy]ethoxy)methyl]-3-nitrobenzene (8.12 g) in DMF (10 ml) was added and the mixture stirred at 20° for 2 h. Phosphate buffer (pH 6.5, 100 ml) and water (100 ml) were added and the product extracted with EtOAc (4×100 ml). The combined organic layer was washed with water (3×100 ml) and dried (Na2SO4). The solvent was removed in vacuo to give a residue that was purified by Biotage. Elution with EtOAc-PE (1:1 then 3:2) followed by solvent evaporation in vacuo gave the title compound (9.50 g). LCMS RT=3.75 min, ES+ve 529 (MH)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198483B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-afa1b2ec95f948feae434e4fbaa3a389
출처 메모uspto-grants-2012_06