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Hydrochloric Acid → 3-Methyl-[1,1'-biphenyl]-2-amine

HRID 485556
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HRID 485556 반응식
[CH3:1][C:2]1[C:3]([N+:14]([O-])=O)=[C:4]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:5]=[CH:6][CH:7]=1.Cl.[OH-].[Na+]>C(O)C>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:3]=1[NH2:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 140439853-Methyl-2-nitro-1,1'-biphenyl

생성물 1

HCID 6030843-Methyl-[1,1'-biphenyl]-2-amine

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

During a 45 minute period 3-methyl-2-nitro-[1,1'-biphenyl] (25.4 g, 0.119 mole) was added portionwise at 30° to a stirred solution of stannous chloride (107.5 g, 0.476 mole) and 150 ml of concentrated hydrochloric acid in enough ethanol to produce a solution. After complete addition the mixture was heated at reflux for 17 hours. The mixture was cooled and made basic (pH 9-10) with 4N aqueous sodium hydroxide, producing a white precipitate. The precipitate was collected by filtration and partitioned between water and methylene chloride. The organic phase was separated, dried over anhydrous magnesium sulfate, and filtered. The filtrate was evaporated to give 3-methyl-[1,1'-biphenyl]-2-amine as a yellow oil.

후처리

  1. customto produce a solution
  2. additionAfter complete addition the mixture
  3. temperaturewas heated
  4. temperatureat reflux for 17 hours
  5. temperatureThe mixture was cooled
  6. customproducing a white precipitate
  7. filtrationThe precipitate was collected by filtration
  8. custompartitioned between water and methylene chloride
  9. customThe organic phase was separated
  10. dry with materialdried over anhydrous magnesium sulfate
  11. filtrationfiltered
  12. customThe filtrate was evaporated

출처 및 근거

ORD 기록
ord-9da9489e2b224fe6907435d0f6466d87
출처 데이터셋
uspto-grants-1985_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04536591

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