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1,4-Dioxane → HCID 57585674, 화합물

HRID 2233342
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HRID 2233342 반응식
[CH2:1]([C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:13]=1[O:12][C:11](=[O:14])[CH:10]=[CH:9]2)[CH:2]=C.[O:15]1CCOCC1>O.O=[Os](=O)(=O)=O>[O:14]=[C:11]1[CH:10]=[CH:9][C:8]2[C:13](=[C:4]([CH2:1][CH:2]=[O:15])[CH:5]=[CH:6][CH:7]=2)[O:12]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 312751,4-DioxaneHCID 4547045HCID 4547045, 화합물

생성물 1

HCID 57585674HCID 57585674, 화합물수율 93%

시약·촉매·용매 2

HCID 30318Osmium Tetroxide촉매HCID 962Water용매2회

실험 절차

To a solution of 8-(2-propen-1-yl)-2H-chromen-2-one (390 mg, 2.0 mmol) in dioxane (10 mL) and water (5 mL) was added OsO4 (4% solution in H2O, 0.5 mL, 10 mol %) and NaIO4 (430 mg, 4.0 mmol). The reaction was stirred at RT for 2 h and NaIO4 (430 mg, 4.0 mmol) was added and the reaction was allowed to stir another 2 h. The reaction was diluted with 20 mL of H2O and was extracted with ethyl acetate (3×50 mL). The combined extracts were dried (Na2SO4), and concentrated to give the title compound (350 mg, 93%) as a dark oil which was used without further purification: MS (ES) m/e 188.9 (M+H)+.

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후처리

  1. stirringto stir another 2 h
  2. extractionwas extracted with ethyl acetate (3×50 mL)
  3. dry with materialThe combined extracts were dried (Na2SO4)
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-e26e4cd89f674e5886c0b50459e9fd5b
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709496B2

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