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Phosphorus oxychloride → 5-Acetyl-3-pyridinecarbonitrile

HRID 2379822
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HRID 2379822 반응식
P(Cl)(Cl)(Cl)=O.[C:6]([C:9]1[CH:10]=[N:11][CH:12]=[C:13]([C:15](=O)[NH2:16])[CH:14]=1)(=[O:8])[CH3:7]>CN(C)C=O>[C:6]([C:9]1[CH:10]=[N:11][CH:12]=[C:13]([C:15]#[N:16])[CH:14]=1)(=[O:8])[CH3:7]
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 226073883-Pyridinecarboxamide, 5-acetyl-

생성물 1

HCID 189537855-Acetyl-3-pyridinecarbonitrile수율 48.5%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Phosphorus oxychloride (2.75 g) was added to a solution of 3-acetyl-5-carbamoylpyridine (2.8 g) in N,N-dimethylformamide (30 ml) with cooling on an ice-water bath. The mixture was stirred with cooling for 1.5 hours. The solvent was removed under reduced pressure. The residue was dissolved in water (150 ml) and the mixture was extracted with ethyl acetate (100 ml). The extract was dried with magnesium sulfate and then evaporated. The residue was chromatographed on a silica gel column eluting with chloroform to afford 3-acetyl-5-cyanopyridine (1.21 g).

후처리

  1. temperaturewith cooling on an ice-water bath
  2. temperaturewith cooling for 1.5 hours
  3. customThe solvent was removed under reduced pressure
  4. dissolutionThe residue was dissolved in water (150 ml)
  5. extractionthe mixture was extracted with ethyl acetate (100 ml)
  6. dry with materialThe extract was dried with magnesium sulfate
  7. customevaporated
  8. customThe residue was chromatographed on a silica gel column
  9. washeluting with chloroform

출처 및 근거

ORD 기록
ord-c7a44f96e5cc4d408dd1ebcf43f7f1f2
출처 데이터셋
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05364871

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