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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Stannous Chloride → N,N-dimethyl-m-phenylenediamine

HRID 244523
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HRID 244523 반응식
[CH3:1][N:2]([CH3:12])[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([N+:9]([O-])=O)[CH:4]=1.[Sn](Cl)Cl>C(O)C>[CH3:1][N:2]([CH3:12])[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([NH2:9])[CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24479Stannous ChlorideHCID 69269N,N-Dimethyl-3-nitroaniline

생성물 1

HCID 76084N,N-dimethyl-m-phenylenediamine수율 82%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

N,N-dimethyl-3-nitroaniline (3.00 g, 18.1 mmol) was dissolved in ethanol (40 cm3). Tin dichloride (16.3 g, 72.0 mmol) was added and the reaction heated under reflux for 16 h. The reaction mixture was allowed to cool before the bulk of the solvent was removed under reduced pressure. The remaining residue was poured in to water (100 cm3), and basified with sodium hydroxide (3M). The mixture was extracted with chloroform (3×30 cm3). The combined extracts were dried over sodium sulphate, filtered and the solvent removed under reduced pressure to give the product as a brown oil (2.01 g, 82%).

후처리

  1. temperaturethe reaction heated
  2. temperatureunder reflux for 16 h
  3. temperatureto cool before the bulk of the solvent
  4. customwas removed under reduced pressure
  5. additionThe remaining residue was poured in to water (100 cm3)
  6. extractionThe mixture was extracted with chloroform (3×30 cm3)
  7. dry with materialThe combined extracts were dried over sodium sulphate
  8. filtrationfiltered
  9. customthe solvent removed under reduced pressure

출처 및 근거

ORD 기록
ord-971757b34e2e402bbe2718b62e4a1ffd
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658665B2

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