Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 503037생성일: 2026년 10월 27일
Phosphate → (5R)-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/503037
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosphate | HCID 1061 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Benzene, 1-(bromomethyl)-3-nitro- | HCID 77568 | — |
| 반응물 | 2-Oxazolidinone, 5-(2,2-diMethyl-4H-1,3-benzodioxin-6-yl)-3-[6-(2-hydroxyethoxy)hexyl]-, (5R)- | HCID 46831955 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (5R)-5-(2,2-Dimethyl-4H-1,3-benzodioxin-6-yl)-3-{6-[2-{(3-nitrophenyl)-methoxy}ethoxy]hexyl}-1,3-oxazolidin-2-one | HCID 46833387 | 37.2% |
반응 단계
A solution of (5R)-5-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-3-[6-(2-hydroxyethoxy)hexyl]-1,3-oxazolidin-2-one (0.20 g) in DMF (5 ml) was treated with sodium hydride (60% dispersion in mineral oil, 0.030 g) and the mixture stirred under nitrogen at 20° C. for 15 min. 3-nitrobenzylbromide (0.111 g) was added, and the mixture stirred at 20° C. for a further 3 h. Phosphate buffer (20 ml, pH6.5) was added and the mixture was stirred for 5 min before extracting with EtOAc (3×20 ml). The organic layer was washed with water (3×20 ml), dried over Na2SO4 and filtered. Solvent evaporation gave the crude product which was purified by flash chromatography on silica. Elution with EtOAc-cyclohexane (7:3) followed by solvent evaporation in vacuo gave the title compound (0.10 g). LCMS RT=3.61 min, ES+ve 529 (MH)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07776895B2 |
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| 출처 데이터셋 | uspto-grants-2010_08 |
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| ORD ID | ord-b9d89219555043a2a2c30482112c0d47 |
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| 출처 메모 | uspto-grants-2010_08 |
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