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Sodium Dithionite → 3-Isobutyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline

HRID 604813
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HRID 604813 반응식
[CH2:1]([C:5]1[CH:6]=[C:7]([CH:9]=[CH:10][CH:11]=1)[NH2:8])[CH:2]([CH3:4])[CH3:3].[F:12][C:13]([F:22])([F:21])[C:14](I)([F:19])[C:15]([F:18])([F:17])[F:16].C(=O)([O-])O.[Na+].S(S([O-])=O)([O-])=O.[Na+].[Na+]>S([O-])(O)(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC.CCCCCC.COC(C)(C)C.O>[CH2:1]([C:5]1[CH:6]=[C:7]([CH:9]=[CH:10][C:11]=1[C:14]([F:19])([C:15]([F:18])([F:17])[F:16])[C:13]([F:22])([F:21])[F:12])[NH2:8])[CH:2]([CH3:4])[CH3:3]
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참가 물질

8

반응물 4

HCID 24489Sodium DithioniteHCID 33978Perfluoroisopropyl iodideHCID 516892Sodium BicarbonateHCID 190247993-Isobutylaniline

생성물 1

HCID 866190023-Isobutyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline수율 47%

시약·촉매·용매 3

HCID 94433
Tetrabutylammonium hydrogen sulfate
촉매
HCID 8058Hexane용매
HCID 23212559water MeOtBu용매

실험 절차

3-Isobutylaniline (14.9 g, 0.1 mol) was diluted in a 300 ml mixed solvent of tert-butyl methyl ether-water (1:1), followed by sequentially adding heptafluoroisopropyl iodide (29.6 g, 0.1 mol), tetrabutylammonium hydrogensulfate (3.4 g, 0.01 mol), sodium hydrogen carbonate (8.4 g, 0.1 mol) and sodium dithionite (17 g, 0.1 mol) and stirring overnight at room temperature. The reaction solution was diluted with hexane, followed by washing twice with a 3N HCl solution, and with aqueous sodium bicarbonate and a saturated brine. The solution was dried over magnesium sulfate and concentrated under reduced pressure, and then the residue was purified by using silica gel chromatography (hexane:ethyl acetate=6:1) to obtain 14.9 g of the desired compound.

후처리

  1. washby washing twice with a 3N HCl solution
  2. dry with materialThe solution was dried over magnesium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customthe residue was purified

출처 및 근거

ORD 기록
ord-de656f68d45a451bb30e7a97ba00655d
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07910735B2

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