반응식
I[C:2]1[Se:3][CH:4]=[CH:5][CH:6]=1.[CH2:7]([O:9][C:10]1[CH:15]=[CH:14][C:13](B(O)O)=[C:12]([F:19])[C:11]=1[F:20])[CH3:8].C(=O)([O-])[O-].[Na+].[Na+]>C1(C)C=CC=CC=1.C(O)C.CC(OC)(C)C>[CH2:7]([O:9][C:10]1[CH:15]=[CH:14][C:13]([C:2]2[Se:3][CH:4]=[CH:5][CH:6]=2)=[C:12]([F:19])[C:11]=1[F:20])[CH3:8]참가 물질
실험 절차
A mixture of 34.8 g (0.14 mol) of 2-iodoselenophene, 32.8 g (0.16 mol) of 4-ethoxy-2,3-difluorophenylboronic acid, 8.10 g (77.01 mmol) of tetrakis -(triphenylphosphine)palladium(0) and 300 ml of 2 N sodium carbonate soln. in 800 ml of toluene/ethanol (1:1) is heated under reflux for 23 h. The mixture is diluted with MTBE and washed with water. The aqueous phase is extracted with MTBE, and the combined organic phases are washed with 2 N hydrochloric acid and sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:EtOAc=15:1-10:1→5:1). Further purification is carried out by recrystallisation from n-heptane; 2-(4-ethoxy-2,3-difluorophenyl)selenophene is obtained as a beige solid.
후처리
- temperatureunder reflux for 23 h
- washwashed with water
- extractionThe aqueous phase is extracted with MTBE
- washthe combined organic phases are washed with 2 N hydrochloric acid and sat. sodium chloride soln
- customThe solution is dried
- concentrationconcentrated to dryness
- customThe residue is purified by column chromatography (SiO2, n-heptane:EtOAc=15:1-10:1→5:1)
- customFurther purification
- customis carried out by recrystallisation from n-heptane
출처 및 근거
- ORD 기록
- ord-0762230a08e74588a5910f25485ffb77
- 출처 데이터셋
- uspto-grants-2012_11
- 특허 번호
- US08304036B2
연결된 노트
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