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Bromide ion → HCID 66771001, 화합물

HRID 1697735
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HRID 1697735 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([F:9])=[CH:4][C:3]=1[CH2:10][C:11]#[N:12].Br[CH2:14][CH2:15]Br.[OH-].[Na+].[Br-]>C1(C)C=CC=CC=1.O>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([F:9])=[CH:4][C:3]=1[C:10]1([C:11]#[N:12])[CH2:15][CH2:14]1
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참가 물질

7

반응물 4

HCID 259Bromide ionHCID 78391,2-DibromoethaneHCID 14798Sodium HydroxideHCID 27740212,4-Dichloro-5-fluorobenzeneacetonitrile

생성물 1

HCID 66771001HCID 66771001, 화합물

시약·촉매·용매 2

HCID 962Water용매
HCID 1140
Toluene
용매

실험 절차

2-(2,4-dichloro-5-fluorophenyl)acetonitrile (1 g, 4.9 mmol, Eq: 1.00) was dissolved in toluene (4 mL). 1,2-Dibromoethane (1.38 g, 634 μL, 7.35 mmol, Eq: 1.50), aqueous NaOH-solution (4.31 mL, 12.5 M; 53.9 mmol, Eq: 11.0) and tertrabutylammonium bromide (348 mg, 1.08 mmol, Eq: 0.22) were added to the above suspension and vigorously stirred at RT for 4 h. The reaction mixture was diluted with water and extracted with AcOEt. The organic solution was washed with 1 N aqueous HCl, then with brine, dried over Na2SO4, filtered and evaporated to dryness. The crude material was purified by flash chromatography (silica gel, 50 g, 0% to 50% EtOAc in heptane) to yield example 461a) (1.13 g; 100%) as an off-white solid. 1H-NMR (CDCl3, 250 MHz) δ [ppm]: 7.51 (1 proton, d, 6.7 Hz); 7.16 (1, proton, d; 8.9 Hz); 1.76-1.80 (2 protons, m); 1.31-1.36 (2 protons, m)

후처리

  1. extractionextracted with AcOEt
  2. washThe organic solution was washed with 1 N aqueous HCl
  3. dry with materialwith brine, dried over Na2SO4
  4. filtrationfiltered
  5. customevaporated to dryness
  6. customThe crude material was purified by flash chromatography (silica gel, 50 g, 0% to 50% EtOAc in heptane)
  7. customto yield example 461a) (1.13 g; 100%) as an off-white solid

출처 및 근거

ORD 기록
ord-db4f08f6b2a3422e810474f7fe6e69ac
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08163793B2

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