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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Selenium Dioxide → (4alphaR,5R,6R,7S)-6,7-Dihydroxy-4alpha,5,6,7-tetrahydro-3,4alpha,5-trimethylnaphtho(2,3-b)furan-2(4H)-one

HRID 1383629
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HRID 1383629 반응식
[OH:1][C@H:2]1[CH2:16][CH:15]=[C:14]2[C@:4]([CH3:17])([CH2:5][C:6]3[C:7](=[CH:13]2)[O:8][C:9](=[O:12])[C:10]=3[CH3:11])[C@H:3]1[CH3:18].[Se](=O)=[O:20]>O1CCOCC1>[OH:1][C@H:2]1[C@@H:16]([OH:20])[CH:15]=[C:14]2[C@:4]([CH3:17])([CH2:5][C:6]3[C:7](=[CH:13]2)[O:8][C:9](=[O:12])[C:10]=3[CH3:11])[C@H:3]1[CH3:18]
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참가 물질

4

반응물 2

HCID 24007Selenium DioxideHCID 10514571HCID 10514571, 화합물

생성물 1

HCID 10084054(4alphaR,5R,6R,7S)-6,7-Dihydroxy-4alpha,5,6,7-tetrahydro-3,4alpha,5-trimethylnaphtho(2,3-b)furan-2(4H)-one수율 86%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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온도
50 °C

실험 절차

The compound prepared in Example B1 (5 mg, 0.02 mmol) was dissolved in dioxane (1 ml), selenium dioxide (22 mg, 0.20 mmol) was added thereto, and the mixture was stirred at 50° C. for 2 days. The reaction solution was filtered, and the solvent was removed by distillation under reduced pressure. The residue was purified by preparative TLC (hexane:ethyl acetate=1:1) to give the title compound (4.5 mg, 86%).

후처리

  1. filtrationThe reaction solution was filtered
  2. customthe solvent was removed by distillation under reduced pressure
  3. customThe residue was purified by preparative TLC (hexane:ethyl acetate=1:1)

출처 및 근거

ORD 기록
ord-519a06bf78c04e78b8b20d3b0ee282a9
출처 데이터셋
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06255339B1

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