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Sodium Hydroxide → 3,5-DIIODOANILINE

HRID 447005
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HRID 447005 반응식
[I:1][C:2]1[CH:7]=[C:6]([N+:8]([O-])=O)[CH:5]=[C:4]([I:11])[CH:3]=1.O.O.Cl[Sn]Cl.[OH-].[Na+]>C(O)C>[I:1][C:2]1[CH:7]=[C:6]([CH:5]=[C:4]([I:11])[CH:3]=1)[NH2:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 61436Stannous chloride dihydrateHCID 121342561,3-Diiodo-5-nitrobenzene

생성물 1

HCID 121342543,5-DIIODOANILINE수율 75.9%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
80 °C

실험 절차

To a solution of 1,3-diiodo-5-nitro-benzene (15.80 g, 0.042 mol) in ethanol (200 mL) was added SnCl2.2H2O (28.50 g, 0.13 mol) portion wise at room temperature. The reaction mixture was heated under reflux at 80° C. for 1.5 h. After cooling to room temperature, the solvent was evaporated under reduced pressure and the crude solid thus obtained was basified with 4N NaOH solution to pH 12. The mixture was extracted with ethyl acetate (×3) and the combined organic layer was washed with brine solution and dried over Na2SO4. The solvent was removed under reduced pressure, to give the desired compound as a yellow solid (11.0 g, 75%).

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureAfter cooling to room temperature
  3. customthe solvent was evaporated under reduced pressure
  4. customthe crude solid thus obtained
  5. extractionThe mixture was extracted with ethyl acetate (×3)
  6. washthe combined organic layer was washed with brine solution
  7. dry with materialdried over Na2SO4
  8. customThe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-3ddcfa1cbdcf41af91a55a40406ec5eb
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08481544B2

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