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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 3106275, 화합물 → 3,5-Dinitropyridine

HRID 617370
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HRID 617370 반응식
[N+:1]([C:4]1[C:5](NN)=[N:6][CH:7]=[C:8]([N+:10]([O-:12])=[O:11])[CH:9]=1)([O-:3])=[O:2]>CO.O.C([O-])(=O)C.[Ag+]>[N+:10]([C:8]1[CH:7]=[N:6][CH:5]=[C:4]([N+:1]([O-:3])=[O:2])[CH:9]=1)([O-:12])=[O:11]
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참가 물질

4

반응물 1

HCID 3106275HCID 3106275, 화합물

생성물 1

HCID 5980543,5-Dinitropyridine수율 21.8%

시약·촉매·용매 2

HCID 11246Silver acetate촉매HCID 22242641Methanol--water (1/1)용매

실험 절차

Silver acetate (2.0 g) was added to a solution of the crude 3,5-dinitro-pyridinyl-hydrazine (2.2 g) in a mixture of methanol:H2O (1:1, 6 ml), and the mixture was stirred at reflux overnight. Solvent was evaporated, then water and conc. NH4OH were added. The mixture was extracted with ethyl ether, the combined extracts were dried over MgSO4, concentrated and purified by column chromatography (5:1 hexane: ethyl acetate) to give the title compound (400 mg) in 21.8% yield. MS (DCI/NH3) m/e: 124 (M-46+1). 1H NMR (CDCl3, 300 MHz) δ: 9.77 (m, 2H), 9.27 (m, 1H).

후처리

  1. temperatureat reflux overnight
  2. customSolvent was evaporated
  3. additionwater and conc. NH4OH were added
  4. extractionThe mixture was extracted with ethyl ether
  5. dry with materialthe combined extracts were dried over MgSO4
  6. concentrationconcentrated
  7. custompurified by column chromatography (5:1 hexane: ethyl acetate)

출처 및 근거

ORD 기록
ord-25ca1739e32740e497785605c05b1fd6
출처 데이터셋
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05948793

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