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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1,4-Dioxane → HCID 12083068, 화합물

HRID 1168847
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HRID 1168847 반응식
[CH2:1]([C:5]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[O:7][N:6]=1)[CH2:2][CH:3]=C.[O:14]1CCOCC1.I([O-])(=O)(=O)=O.[Na+]>[Os](=O)(=O)(=O)=O.O.C(OCC)(=O)C>[O:7]1[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:5]([CH2:1][CH2:2][CH:3]=[O:14])=[N:6]1
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참가 물질

7

반응물 3

HCID 312751,4-DioxaneHCID 12083067HCID 12083067, 화합물HCID 23667635Sodium periodate

생성물 1

HCID 12083068HCID 12083068, 화합물

시약·촉매·용매 3

HCID 30318Osmium Tetroxide촉매HCID 962Water용매2회
HCID 8857
Ethyl Acetate
용매

실험 절차

Compound 26 (549 mg, 3.2 mmol), water (5 mL), 1,4-dioxane (15 mL) and osmium tetroxide (15 mg, 0.06 mmol) were stirred for 5 min. in a small flask. Sodium metaperiodate (1.56 g, 7.3 mmol) was added over 30 min. and the suspension was then stirred for 1 hour. Ethyl acetate and water were added. The phases were separated and the aqueous phase was extracted with ethyl acetate and dichloromethane. The combined organic phases were dried over magnesium sulphate and evaporated to dryness to produce 784 mg of crude 27, which was used directly without further purification in the synthesis compound 28.

후처리

  1. customThe phases were separated
  2. extractionthe aqueous phase was extracted with ethyl acetate and dichloromethane
  3. dry with materialThe combined organic phases were dried over magnesium sulphate
  4. customevaporated to dryness
  5. customto produce 784 mg of crude 27, which
  6. customwas used directly without further purification in the synthesis compound 28

출처 및 근거

ORD 기록
ord-16cbe03f2e3744d1a53ad3cfe2498431
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06627645B2

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