Ethanol → 3-Ethenyl-2,6-difluorobenzonitrile

HRID 2175835노트

반응식

HRID 2175835 반응식
FC(F)(F)S(O[C:7]1[CH:12]=[CH:11][C:10]([F:13])=[C:9]([C:14]#[N:15])[C:8]=1[F:16])(=O)=O.[CH2:19](O)[CH3:20]>C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C(Cl)Cl>[CH:19]([C:7]1[C:8]([F:16])=[C:9]([C:10]([F:13])=[CH:11][CH:12]=1)[C:14]#[N:15])=[CH2:20]

참가 물질

4

반응물 2

HCID 702EthanolHCID 867270593-Cyano-2,4-difluorophenyl trifluoromethanesulfonate

생성물 1

HCID 867270603-Ethenyl-2,6-difluorobenzonitrile

시약·촉매·용매 1

HCID 178418807HCID 178418807, 화합물촉매

실험 절차

3-Cyano-2,4-difluorophenyl trifluoromethanesulfonate (5.20 g, 18.1 mmol), potassium vinyl trifluoroborate (4.85 g, 36.2 mmol), PdCl2(dppf)-CH2Cl2 Adduct (0.662 g, 0.905 mmol), and TEA (5.05 mL, 36.2 mmol) were added to 75 mL of ethanol. The reaction mixture was degassed then heated at reflux for 4 h. LC-MS analysis confirmed product peak. The reaction mixture was diluted with ethyl acetate, washed twice with brine, dried, and evaporated to dryness. The crude material was then purified by MPLC chromatography through a 330 g Redi-sep column eluting with 10% EtOAc/Hexane solvent system to yield 3-ethenyl-2,6-difluorobenzonitrile.

후처리

  1. customThe reaction mixture was degassed
  2. temperaturethen heated
  3. temperatureat reflux for 4 h
  4. additionThe reaction mixture was diluted with ethyl acetate
  5. washwashed twice with brine
  6. customdried
  7. customevaporated to dryness
  8. customThe crude material was then purified by MPLC chromatography through a 330 g Redi-sep column
  9. washeluting with 10% EtOAc/Hexane solvent system

출처 및 근거

ORD 기록
ord-757af68304c14e249a9cf72079d3ce52
출처 데이터셋
uspto-grants-2015_06
특허 번호
US09062070B2

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