Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1043884생성일: 2026년 10월 26일
3,6-Dioxabicyclo[3.1.0]hexane → t-butyl 2-((3RS,4SR)-4-hydroxytetrahydrofuran-3-yl)hydrazinecarboxylate
https://huagongshe.com/reaction/1043884
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3,6-Dioxabicyclo[3.1.0]hexane | HCID 67511 | — |
| 반응물 | tert-Butyl carbazate | HCID 70091 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | t-butyl 2-((3RS,4SR)-4-hydroxytetrahydrofuran-3-yl)hydrazinecarboxylate | HCID 86686323 | — |
반응 단계
3,4-epoxytetrahydrofuran (3.33 mL) and t-butyl carbazate (6.14 g) were dissolved in 2-propanol (15 mL), and the solution was heated to 90° C. After three days, t-butyl carbazate (6.3 g) was further added. After heating with stirring for further two days, the reaction mixture was cooled to room temperature and concentrated under reduced pressure. Xylene was added to the residue, and the mixture was concentrated again under reduced pressure. The residue was partitioned by adding chloroform and brine. The organic layer was dried over anhydrous magnesium sulfate. The desiccant was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate/n-heptane, 50% to 100%) to give the title compound (5.78 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08563565B2 |
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| 출처 데이터셋 | uspto-grants-2013_10 |
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| ORD ID | ord-5658e5329f584198ac6b9c3d1df16b94 |
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| 출처 메모 | uspto-grants-2013_10 |
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