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Sodium Hydroxide → (2-Amino-3-chlorophenyl)amine

HRID 240353
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HRID 240353 반응식
[Cl:1][C:2]1[C:3]([N+:9]([O-])=O)=[C:4]([CH:6]=[CH:7][CH:8]=1)[NH2:5].O.O.[Sn](Cl)Cl.[OH-].[Na+]>CO.Cl>[Cl:1][C:2]1[C:3]([NH2:9])=[C:4]([NH2:5])[CH:6]=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 14798Sodium HydroxideHCID 61436Stannous chloride dihydrateHCID 1010683-Chloro-2-nitroaniline

생성물 1

HCID 3462489(2-Amino-3-chlorophenyl)amine수율 101.7%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 887Methanol용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

12.5 g (72.4 mmol) of 3-chloro-2-nitroaniline was dissolved in methanol (250 ml), and a solution prepared by dissolving 57.2 g (253 mmol) of tin (II) chloride dihydrate in concentrated hydrochloric acid (75 mL) was added dropwise. The reaction mixture was heated with stirring for 3 hours, and concentrated under reduced pressure. Water was added to the residue thus obtained, and the solution was alkalinized with a 25% aqueous solution of sodium hydroxide, and extracted with methylene chloride. The extracted organic layer was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure, to obtain 10.5 g (yield: >99%) of 3-chloro-1,2-phenylenediamine as a pale magenta-colored liquid.

후처리

  1. customa solution prepared
  2. additionwas added dropwise
  3. temperatureThe reaction mixture was heated
  4. concentrationconcentrated under reduced pressure
  5. additionWater was added to the residue
  6. customthus obtained
  7. extractionextracted with methylene chloride
  8. dry with materialThe extracted organic layer was dried over anhydrous magnesium sulfate
  9. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-830a6c4297cc485a9898edc0f36e3fe1
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08648075B2

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