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N-(2-Methoxyethyl)-2-nitroaniline → 1-N-(2-methoxyethyl)benzene-1,2-diamine

HRID 1096655
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HRID 1096655 반응식
[CH3:1][O:2][CH2:3][CH2:4][NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[N+:12]([O-])=O>CO.C(O)(=O)C.[Zn]>[CH3:1][O:2][CH2:3][CH2:4][NH:5][C:6]1[C:7]([NH2:12])=[CH:8][CH:9]=[CH:10][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 10375425N-(2-Methoxyethyl)-2-nitroaniline

생성물 1

HCID 102614521-N-(2-methoxyethyl)benzene-1,2-diamine수율 72%

시약·촉매·용매 3

HCID 23994Zinc촉매HCID 176Acetic Acid용매HCID 887Methanol용매

실험 절차

The residue 109A was dissolved in methanol (60 mL) and acetic acid (4 mL). Zinc metal (3.24 g, 49.6 mmol) was added and the mixture was stirred overnight at room temperature. The reaction was decanted off from unreacted zinc metal. The solvent was removed under vacuum and resuspended in ethyl acetate (30 mL). The precipitate was removed by filtration on a Buchner funnel with Celite. Solvent was removed from the filtrate and the residue was purified by column chromatography (2% MeOH/DCM) to give the product N1-(2-methoxyethyl)benzene-1,2-diamine (109B) as a red oil (422 mg, 72% yield over two steps). ESI-MS:m/z 167.4 (M+H)+.

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후처리

  1. customThe reaction was decanted off from unreacted zinc metal
  2. customThe solvent was removed under vacuum
  3. customThe precipitate was removed by filtration on a Buchner funnel with Celite
  4. customSolvent was removed from the filtrate
  5. customthe residue was purified by column chromatography (2% MeOH/DCM)

출처 및 근거

ORD 기록
ord-46108410ddf843bca44d8d93e7125b22
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08138168B1

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