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Dimethylformamide → 2,6-Dibromo-1,4-phenylenediamine

HRID 1600677
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HRID 1600677 반응식
[Br:1][C:2]1[CH:8]=[C:7]([N+:9]([O-])=O)[CH:6]=[C:5]([Br:12])[C:3]=1[NH2:4].C(OCC)(=O)C.CN(C)C=O.[H][H]>C(O)C.[Pt]>[NH2:4][C:3]1[C:2]([Br:1])=[CH:8][C:7]([NH2:9])=[CH:6][C:5]=1[Br:12]
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참가 물질

7

반응물 4

HCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 132312,6-Dibromo-4-nitroanilineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 6533412,6-Dibromo-1,4-phenylenediamine

시약·촉매·용매 2

HCID 23939Platinum촉매HCID 702Ethanol용매

실험 절차

3.0 g of 2,6-dibromo-4-nitroaniline are dissolved in 150 ml of ethanol, 150 ml of ethyl acetate and 30 ml of dimethylformamide and, after addition of 0.5 g of platinum on carbon (5%), hydrogenated under a pressure of 1.5 bar of hydrogen in a Parr apparatus at room temperature for 1 hour. Cooling is followed by filtration, the solvent is distilled off in a rotary evaporator, and the residue is purified by column chromatography.

후처리

  1. temperatureCooling
  2. filtrationis followed by filtration
  3. distillationthe solvent is distilled off in a rotary evaporator
  4. customthe residue is purified by column chromatography

출처 및 근거

ORD 기록
ord-b1ee345baeaf4d92a55db75fab27a8a9
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05977102

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