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Ethanol → 2-Amino-2-methyl-4-(2-trifluoromethylphenyl)butyronitrile

HRID 9929
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HRID 9929 반응식
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH2:10]C(=O)C.[C-:16]#[N:17].[Na+].[Cl-].[NH4+:20].[CH2:21](O)[CH3:22]>N>[NH2:20][C:21]([CH3:22])([CH2:10][CH2:9][C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=1[C:2]([F:15])([F:14])[F:1])[C:16]#[N:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 702EthanolHCID 8929Sodium CyanideHCID 25517Ammonium ChlorideHCID 117460214-[2-(Trifluoromethyl)phenyl]butan-2-one

생성물 1

HCID 112187182-Amino-2-methyl-4-(2-trifluoromethylphenyl)butyronitrile

시약·촉매·용매 1

HCID 222Ammonia용매

실험 절차

1.5 g of 4-(2-trifluoromethylphenyl)butan-2-one, 0.41 g of sodium cyanide and 0.56 g of ammonium chloride are dissolved in 77 ml of a 2M solution of ammonia in ethanol and the mixture is stirred at ambient temperature for 7 h. The mixture is subsequently concentrated under reduced pressure and the residue is redissolved in ethyl acetate and washed with water and three times with saturated sodium chloride solution. The organic phase is separated, dried with magnesium sulfate and evaporated under reduced pressure. After purifying the residue by flash chromatography, the title compound is thus obtained.

후처리

  1. concentrationThe mixture is subsequently concentrated under reduced pressure
  2. dissolutionthe residue is redissolved in ethyl acetate
  3. washwashed with water and three times with saturated sodium chloride solution
  4. customThe organic phase is separated
  5. dry with materialdried with magnesium sulfate
  6. customevaporated under reduced pressure
  7. customAfter purifying the residue by flash chromatography

출처 및 근거

ORD 기록
ord-f7bffe1edf2743528fa2a6dad5094133
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07091371B2

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