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

HRID 1472758

반응식

HRID 1472758 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

반응 조건

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 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-9ca52b1ab4a14db4bc0d26e44586abdf
출처 데이터셋
uspto-grants-2015_04
특허 번호
US09012654B2

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