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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dimethylformamide → 2,6-Dibromo-1,4-phenylenediamine

HRID 725833
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HRID 725833 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>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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 132312,6-Dibromo-4-nitroaniline

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-nitro-aniline 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-charcoal (5%), are hydrogenated in a Parr apparatus at room temperature under a hydrogen pressure of 1.5 bar for 1 hour. After cooling, the mixture is filtered, the solvent is distilled off in a rotary evaporator and the residue is purified by column chromatography.

후처리

  1. customare hydrogenated in a Parr apparatus at room temperature under a hydrogen
  2. customfor 1 hour
  3. temperatureAfter cooling
  4. filtrationthe mixture is filtered
  5. distillationthe solvent is distilled off in a rotary evaporator
  6. customthe residue is purified by column chromatography

출처 및 근거

ORD 기록
ord-8b2f955d9d184db98e857024beb0a8d0
출처 데이터셋
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05707989

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