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1,3,5-Triazine → 1-(3-Nitrophenyl)-1H-1,2,4-triazole

HRID 2086798
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HRID 2086798 반응식
Cl.[N+:2]([C:5]1[CH:6]=[C:7]([NH:11][NH2:12])[CH:8]=[CH:9][CH:10]=1)([O-:4])=[O:3].[N:13]1[CH:18]=NC=N[CH:14]=1.C(=O)(O)[O-].[Na+]>C(O)C>[N+:2]([C:5]1[CH:6]=[C:7]([N:11]2[CH:18]=[N:13][CH:14]=[N:12]2)[CH:8]=[CH:9][CH:10]=1)([O-:4])=[O:3]
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참가 물질

5

반응물 3

HCID 92621,3,5-TriazineHCID 516892Sodium BicarbonateHCID 54642853-Nitrophenylhydrazinium(1+) chloride

생성물 1

HCID 149508381-(3-Nitrophenyl)-1H-1,2,4-triazole수율 49.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 3-nitrophenylhydrazine hydrochloride (8.77 g) and 1,3,5-triazine (2.50 g) in ethanol (40 ml) was stirred under reflux for 4 hours. Then the mixture was poured into aqueous sodium bicarbonate and extracted with ethyl acetate twice. The combined organic phase was washed with aqueous sodium bicarbonate and brine, dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel column (hexane-ethyl acetate, 3:7) to give 1-(3-nitrophenyl)-1H-1,2,4-triazole (2.89 g) as a solid.

후처리

  1. temperatureunder reflux for 4 hours
  2. extractionextracted with ethyl acetate twice
  3. washThe combined organic phase was washed with aqueous sodium bicarbonate and brine
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated
  6. customThe residue was chromatographed on silica gel column (hexane-ethyl acetate, 3:7)

출처 및 근거

ORD 기록
ord-cc6b3a560c9b40168ddbcd3fe480e95b
출처 데이터셋
uspto-grants-2004_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06727245B2

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