Tributylvinyltin → Ethyl 4-fluoro-3-vinylbenzoate
반응식
Br[C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[F:13])[C:5]([O:7][CH2:8][CH3:9])=[O:6].[CH3:14][CH2:15]CC[Sn](C=C)(CCCC)CCCC.[F-].[K+]>O1CCOCC1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Pd]Cl>[F:13][C:12]1[CH:11]=[CH:10][C:4]([C:5]([O:7][CH2:8][CH3:9])=[O:6])=[CH:3][C:2]=1[CH:14]=[CH2:15]참가 물질
실험 절차
A mixture of compound ethyl 3-bromo-4-fluorobenzoate (Preparation 53, 81 g, 328.8 mmol, 1 eq) and bis(triphenylphosphine)palladium (II) chloride (7 g, 9.9 mmol, 0.03 eq) in dioxane (600 mL) was charged with nitrogen. Tin vinyltributyl (115 g, 361.6 mmol, 1.10 eq) was added and the mixture was heated to reflux overnight. The mixture was filtrated and the filtrate was concentrated in vacuum. The residue was dissolved in ether (2 L) and water (1 L). Then potassium fluoride (10 g, 1.7 mol, 5.17 eq) was added to the mixture and much of solid precipitated. The mixture was filtrated and the filtrate was separated. The aqueous phase was extracted with ether (200 mL×2). The combined organic phases were washed with brine, dried over sodium sulfate and concentrated in vacuo to give a residue. The residue was purified by chromatography (petroleum ether) to title compound as a colorless oil (55.8 g, 286 mmol, 87%).
후처리
- additionwas charged with nitrogen
- temperaturethe mixture was heated
- temperatureto reflux overnight
- filtrationThe mixture was filtrated
- concentrationthe filtrate was concentrated in vacuum
- dissolutionThe residue was dissolved in ether (2 L)
- customprecipitated
- filtrationThe mixture was filtrated
- customthe filtrate was separated
- extractionThe aqueous phase was extracted with ether (200 mL×2)
- washThe combined organic phases were washed with brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated in vacuo
- customto give a residue
출처 및 근거
- ORD 기록
- ord-efcf117a2b7449049912b332ae2ec50c
- 출처 데이터셋
- uspto-grants-2013_01
- 특허 번호
- US08357711B2
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