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Sodium Hydroxide → 3,5-DIIODOANILINE

HRID 447005
ノート
印刷プレビュー

反応式

HRID 447005 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 121342543,5-DIIODOANILINE収率 75.9%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
80 °C

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-3ddcfa1cbdcf41af91a55a40406ec5eb
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08481544B2

反応ノート

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