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Water → 5-Bromo-6-methylpyridine-2-carbonitrile

HRID 717161
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HRID 717161 반응식
[Br:1][C:2]1[C:3]([CH3:9])=[N:4][C:5](Br)=[CH:6][CH:7]=1.[Cu][C:11]#[N:12].CN(C)C=O.O>C(OCC)(=O)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:11]#[N:12])=[N:4][C:3]=1[CH3:9]
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참가 물질

6

반응물 4

HCID 962WaterHCID 6228DimethylformamideHCID 27629463,6-Dibromo-2-methylpyridineHCID 178418546HCID 178418546, 화합물

생성물 1

HCID 498187795-Bromo-6-methylpyridine-2-carbonitrile수율 49%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
110 °C

실험 절차

3,6-Dibromo-2-methylpyridine (4.9 g, 19.53 mmol), copper(I)cyanide (1.75 g, 19.53 mmol) and N,N-dimethylformamide (20 mL) were combined in a sealable vessel with a stirbar. The resulting mixture was sealed, stirred vigorously and heated at 110° C. for 4 h. The resulting mixture was diluted with ethyl acetate, poured into a separatory funnel containing water and the layers were separated. The water layer was extracted with ethyl acetate twice. The combined organics were washed with brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The resulting solid was purified by silica gel chromatography (10% ethyl acetate in hexanes) to give the title compound as a white solid (1.88 g, 9.54 mmol, 49% yield). MS (ESI) m/z 197.3 [M]+.

후처리

  1. customThe resulting mixture was sealed
  2. additionpoured into a separatory funnel
  3. customthe layers were separated
  4. extractionThe water layer was extracted with ethyl acetate twice
  5. washThe combined organics were washed with brine
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe resulting solid was purified by silica gel chromatography (10% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-93e08671759b46fe9a5d27300bf34941
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09193692B2

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