Sodium Carbonate → 4-(4-Isopropylphenyl)pyridine

HRID 628832노트

반응식

HRID 628832 반응식
Cl.Br[C:3]1[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=1.[CH:9]([C:12]1[CH:17]=[CH:16][C:15](B(O)O)=[CH:14][CH:13]=1)([CH3:11])[CH3:10].C(=O)([O-])[O-].[Na+].[Na+]>C(#N)C.O>[CH:9]([C:12]1[CH:17]=[CH:16][C:15]([C:3]2[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=2)=[CH:14][CH:13]=1)([CH3:11])[CH3:10]

참가 물질

5

실험 절차

Part A. A solution of 4-bromopyridine hydrochloride (1.0 g, 6.3 mmol) in acetonitrile-water (50 mL/20 mL) is treated with 4-isopropylbenzeneboronic acid (1.04 g, 6.3 mmol) and sodium carbonate (2.1 g, 25.2 mmol). The mixture is degassed twice, and a catalytic quantity of tetrakis(triphenylphosphine)palladium is added. The mixture is heated to reflux for 12 h., then cooled and poured into water (50 mL). The mixture is filtered and extracted with ethyl acetate (3×50 mL). The extracts are combined, washed with brine, dried over magnesium sulfate, filtered and evaporated to afford 1.01 g of sufficiently pure product, 4-(4-isopropyl-phenyl)-pyridine.

후처리

  1. customThe mixture is degassed twice
  2. additiona catalytic quantity of tetrakis(triphenylphosphine)palladium is added
  3. temperatureThe mixture is heated
  4. temperatureto reflux for 12 h.
  5. temperaturecooled
  6. additionpoured into water (50 mL)
  7. filtrationThe mixture is filtered
  8. extractionextracted with ethyl acetate (3×50 mL)
  9. washwashed with brine
  10. dry with materialdried over magnesium sulfate
  11. filtrationfiltered
  12. customevaporated

출처 및 근거

ORD 기록
ord-9ccb15b898d346b8b3265b38e81e11f7
출처 데이터셋
uspto-grants-2016_04
특허 번호
US09315467B2

반응 노트

불러오는 중…