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Stannous chloride dihydrate → 1-(3,4-diaminophenyl)ethanone

HRID 555422
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HRID 555422 반응식
[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][C:7]([NH2:10])=[C:6]([N+:11]([O-])=O)[CH:5]=1)=[O:3].O.O.Cl[Sn]Cl.C([O-])(O)=O.[Na+]>CCOC(C)=O.O>[NH2:11][C:6]1[CH:5]=[C:4]([C:2](=[O:3])[CH3:1])[CH:9]=[CH:8][C:7]=1[NH2:10]
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참가 물질

6

반응물 3

HCID 61436Stannous chloride dihydrateHCID 516892Sodium BicarbonateHCID 115863891-(4-amino-3-nitrophenyl)ethanone

생성물 1

HCID 4327231-(3,4-diaminophenyl)ethanone

시약·촉매·용매 2

HCID 962Water용매HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 4-methylcarbonyl-2-nitro-benzenamine (500 mg, 2.775 mmol) in EtOAc (16 mL) was added SnCl2.2H2O (3.130 g, 13.88 mmol). The reaction mixture was refluxed for 2.5 h, cooled to rt, and diluted with H2O (130 mL). The pH of the mixture was adjusted to 7-8 by addition of saturated NaHCO3 solution and the aqueous phase was extracted with EtOAc (2×120 mL). The combined organic extracts were washed with brine (2×60 mL) and dried over MgSO4. After the removal of the solvent under vacuum, 142a was obtained as a red orange solid (418 mg).

후처리

  1. temperatureThe reaction mixture was refluxed for 2.5 h
  2. extractionthe aqueous phase was extracted with EtOAc (2×120 mL)
  3. washThe combined organic extracts were washed with brine (2×60 mL)
  4. dry with materialdried over MgSO4
  5. customAfter the removal of the solvent under vacuum

출처 및 근거

ORD 기록
ord-ca0b7a9dd9b24df397a66ed41808e721
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08053450B2

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