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

HRID 53808
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HRID 53808 반응식
[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
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참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-b0f87a1b3f1f410ca61a6fe6a8fdbc6c
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05620979

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