m-Anisoyl chloride → 4-Chloro-2-fluoro-6-(3-methoxybenzoyl)benzonitrile

HRID 1662223

반응식

HRID 1662223 반응식
Br[C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[C:6]([F:11])[C:3]=1[C:4]#[N:5].[Br-].[Li+].[Cu]C#N.[CH3:17][O:18][C:19]1[CH:20]=[C:21]([CH:25]=[CH:26][CH:27]=1)[C:22](Cl)=[O:23]>C1COCC1.[Zn]>[Cl:10][C:8]1[CH:9]=[C:2]([C:22](=[O:23])[C:21]2[CH:25]=[CH:26][CH:27]=[C:19]([O:18][CH3:17])[CH:20]=2)[C:3]([C:4]#[N:5])=[C:6]([F:11])[CH:7]=1

참가 물질

7

실험 절차

2-Bromo-4-chloro-6-fluorobenzonitrile (6.95 g, 29.64 mmol) was dissolved in THF (15 mL) and added to a bottle of Rieke® Zinc in THF (50 mg/mL, 50.0 mL, 38.24 mmol) at 0° C. under an argon atmosphere. The resulting mixture was stirred at rt for 6 h and then stored in a refrigerator for 60 h allowing the excess of zinc to settle. The solution was carefully decanted off and cooled to −78° C. under an argon atmosphere. A solution of lithium bromide (5.15 g, 59.28 mmol) and copper(I) cyanide (2.65 g, 29.64 mmol) in THF (30 mL) was added and the resulting mixture was stirred at rt for 30 min. The mixture was cooled to −78° C. and then 3-methoxybenzoyl chloride (4.17 mL, 29.64 mmol) was added dropwise. The cooling bath was removed and the resulting mixture was stirred at rt for 1.5 h. Saturated aqueous NH4Cl (12 mL) was added to the mixture, the THF was removed in vacuo and the residue was diluted with water (50 mL) and DCM (50 mL). The mixture was poured into a phase separator, the organic phase was collected, concentrated and purified on a silica gel column (0-30% EtOAc in heptane) to give 4.7 g (55%) of the title compound.

후처리

  1. waitstored in a refrigerator for 60 h
  2. customThe solution was carefully decanted off
  3. temperaturecooled to −78° C. under an argon atmosphere
  4. stirringthe resulting mixture was stirred at rt for 30 min
  5. temperatureThe mixture was cooled to −78° C.
  6. customThe cooling bath was removed
  7. stirringthe resulting mixture was stirred at rt for 1.5 h
  8. additionSaturated aqueous NH4Cl (12 mL) was added to the mixture
  9. customthe THF was removed in vacuo
  10. additionthe residue was diluted with water (50 mL) and DCM (50 mL)
  11. additionThe mixture was poured into a phase separator
  12. customthe organic phase was collected
  13. concentrationconcentrated
  14. custompurified on a silica gel column (0-30% EtOAc in heptane)

출처 및 근거

ORD 기록
ord-e6852b5321c84dbb9f7c3449ee6208b3
출처 데이터셋
uspto-grants-2011_10
특허 번호
US08030500B2

연결된 노트

불러오는 중…