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4-Bromo-2,6-dimethylquinoline → 4-Cyano-2,6-dimethylquinoline

HRID 1581453
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HRID 1581453 반응식
Br[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([CH3:12])[CH:10]=2)[N:5]=[C:4]([CH3:13])[CH:3]=1.[C:14]([Cu])#[N:15]>CN(C=O)C>[C:14]([C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([CH3:12])[CH:10]=2)[N:5]=[C:4]([CH3:13])[CH:3]=1)#[N:15]
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참가 물질

4

반응물 2

HCID 149913604-Bromo-2,6-dimethylquinolineHCID 178418546HCID 178418546, 화합물

생성물 1

HCID 149913674-Cyano-2,6-dimethylquinoline수율 55.5%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

First, 4-bromo-2,6-dimethylquinoline (5.0 g) and CuCN (4.82 g) were added to DMF (70 ml) and were allowed to react for 6 hours at a temperature of 140° C. Ice was poured to the reaction solution and the produced precipitate was removed through filtering. The filtrate was extracted using ethyl acetate, the solvent was removed under reduced pressure, and the residue was purified through column chromatography (silica gel, hexane/ethyl acetate=4/1) to obtain 4-cyano-2,6-dimethylquinoline (2.14 g) represented by the following chemical formula (47).

후처리

  1. customto react for 6 hours at a temperature of 140° C
  2. additionIce was poured to the reaction solution
  3. customthe produced precipitate was removed
  4. filtrationthrough filtering
  5. extractionThe filtrate was extracted
  6. customthe solvent was removed under reduced pressure
  7. customthe residue was purified through column chromatography (silica gel, hexane/ethyl acetate=4/1)

출처 및 근거

ORD 기록
ord-ace30e94cb794f45b8109612a8052ec2
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06730418B2

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