Water → 3-Pyridinecarbonitrile, 6-(chlorodifluoromethyl)-

HRID 217253

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HRID 217253 반응식
[Cl:1][C:2]([F:11])([F:10])[C:3](=O)/[CH:4]=[CH:5]/OCC.C[N:13](C)[CH:14]=[CH:15][C:16]#[N:17].C([O-])(=O)C.[NH4+].O>C1(C)C=CC=CC=1>[Cl:1][C:2]([F:10])([F:11])[C:3]1[CH:4]=[CH:5][C:15]([C:16]#[N:17])=[CH:14][N:13]=1

참가 물질

6

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온도
100 °C

실험 절차

(3E)-1-Chloro-4-ethoxy-1,1-difluorobut-3-en-2-one (7.36 g, 40 mmol) was dissolved in dry toluene (40 mL) and treated with 3-dimethylaminoacrylonitrile (4.61 g, 48 mmol) at room temperature. The solution was heated at about 100° C. for 3.5 hr. The solvent was then removed under reduced pressure and the remaining mixture was re-dissolved in DMF (20 mL), treated with ammonium acetate (4.62 g, 60 mmol) and stirred at room temperature overnight. Water was added to the reaction mixture and the resulting mixture was extracted with ether-CH2CH2 (1:2, v/v) twice. The combined organic layer was washed with brine, dried, filtered and concentrated. The residue was purified on silica gel to give 3.1 g of 6-[chloro(difluoro)methyl]nicotinonitrile (A) as light colored oil in 41% yield. GC-MS: mass calcd for C7H3ClF2N2 [M]+ 188. Found 188.

후처리

  1. customThe solvent was then removed under reduced pressure
  2. dissolutionthe remaining mixture was re-dissolved in DMF (20 mL)
  3. extractionthe resulting mixture was extracted with ether-CH2CH2 (1:2
  4. washThe combined organic layer was washed with brine
  5. customdried
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was purified on silica gel

출처 및 근거

ORD 기록
ord-b9ef8a88495e478590e57a65bfb76b2f
출처 데이터셋
uspto-grants-2012_06
특허 번호
US08193364B2

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