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Isobutyronitrile → 2-(6-Bromopyridin-2-yl)-2-methylpropanenitrile

HRID 384047
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HRID 384047 반응식
C[Si]([N-][Si](C)(C)C)(C)C.[K+].[C:11](#[N:15])[CH:12]([CH3:14])[CH3:13].Br[C:17]1[CH:22]=[CH:21][CH:20]=[C:19]([Br:23])[N:18]=1>C1(C)C=CC=CC=1.CCOCC>[Br:23][C:19]1[N:18]=[C:17]([C:12]([CH3:14])([CH3:13])[C:11]#[N:15])[CH:22]=[CH:21][CH:20]=1
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참가 물질

6

반응물 3

HCID 6559IsobutyronitrileHCID 122742,6-DibromopyridineHCID 3251421Potassium bis(trimethylsilyl)amide

생성물 1

HCID 579696582-(6-Bromopyridin-2-yl)-2-methylpropanenitrile수율 65.5%

시약·촉매·용매 2

HCID 1140Toluene용매2회HCID 3283Diethyl Ether
용매

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온도
0 °C

실험 절차

Potassium bis(trimethylsilyl)amide (0.5 M in toluene, 200 ml, 100 mmol) was added slowly to a solution of isobutyronitrile (8.55 ml, 95.26 mmol) in toluene (200 ml) cooled down to 0° C. After complete addition, the reaction mixture was allowed to warm up to room temperature over 1 hour. The resulting mixture was added to a solution of 2,6-dibromopyridine (56.42 g, 238.15 mmol) in toluene (100 ml). The reaction mixture was stirred at room temperature for 18 hours. The crude mixture was diluted with ether, washed with a saturated aqueous solution of ammonium chloride and brine. The organic phase was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified on silica gel by flash column chromatography to afford the title compound as an oil (14.04 g, 65% yield).

후처리

  1. additionAfter complete addition
  2. temperatureto warm up to room temperature over 1 hour
  3. washwashed with a saturated aqueous solution of ammonium chloride and brine
  4. dry with materialThe organic phase was dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified on silica gel by flash column chromatography

출처 및 근거

ORD 기록
ord-ccc80749565e4d3a8e5cc79fee5e0763
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367697B2

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