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Stannous Chloride → 4,5-Bis(trifluoromethyl)benzene-1,2-diamine

HRID 53808
ノート
印刷プレビュー

反応式

HRID 53808 の反応式
[F:1][C:2]([F:18])([F:17])[C:3]1[C:9]([C:10]([F:13])([F:12])[F:11])=[CH:8][C:6]([NH2:7])=[C:5]([N+:14]([O-])=O)[CH:4]=1.Cl[Sn]Cl>C(O)C>[F:1][C:2]([F:17])([F:18])[C:3]1[C:9]([C:10]([F:13])([F:12])[F:11])=[CH:8][C:6]([NH2:7])=[C:5]([NH2:14])[CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24479Stannous ChlorideHCID 47376332-Nitro-4,5-bis(trifluoromethyl)aniline

生成物 1

HCID 40613654,5-Bis(trifluoromethyl)benzene-1,2-diamine収率 94%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

p A solution of 122 mg (0.445 mmol) of 4,5-bis(trifluoromethyl)-2-nitroaniline and 498 mg (2.62 mmol) of SnCl2 in 6 mL of ethanol was heated at 70° C. for 2 h. The solution was evaporated to remove the ethanol. The residue was treated with 2 N NaOH to pH=13. White precipitate was observed. The mixture was extracted by CHCl3 (3×10 mL). The extract was dried (MgSO4) and evaporated to leave 102 mg (94% ) of oil. 1H NMR (CDCl3), 3.70 (mb, 4), 7.069 (s, 2) and some impurity. 19F NMR (CDCl3), 56.659 (s).

後処理

  1. customThe solution was evaporated
  2. customto remove the ethanol
  3. additionThe residue was treated with 2 N NaOH to pH=13
  4. extractionThe mixture was extracted by CHCl3 (3×10 mL)
  5. dry with materialThe extract was dried (MgSO4)
  6. customevaporated

出典と根拠

ORDレコード
ord-b0f87a1b3f1f410ca61a6fe6a8fdbc6c
出典データセット
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05620979

反応ノート

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