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]=1참가 물질
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
- waitstored in a refrigerator for 60 h
- customThe solution was carefully decanted off
- temperaturecooled to −78° C. under an argon atmosphere
- stirringthe resulting mixture was stirred at rt for 30 min
- temperatureThe mixture was cooled to −78° C.
- customThe cooling bath was removed
- stirringthe resulting mixture was stirred at rt for 1.5 h
- additionSaturated aqueous NH4Cl (12 mL) was added to the mixture
- customthe THF was removed in vacuo
- additionthe residue was diluted with water (50 mL) and DCM (50 mL)
- additionThe mixture was poured into a phase separator
- customthe organic phase was collected
- concentrationconcentrated
- 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
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