Cesium fluoride → HCID 24825942、化合物
反応式
Br[CH:2]=[C:3]1[O:7][C:6](=[O:8])[CH:5]=[CH:4]1.[F:9][C:10]1[CH:15]=[CH:14][C:13](B(O)O)=[CH:12][CH:11]=1.[F-].[Cs+]>[I-].C([N+](CCCC)(CCCC)CCCC)CCC.C1(C)C=CC=CC=1.O.[Cl-].[Na+].O.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[F:9][C:10]1[CH:15]=[CH:14][C:13](/[CH:2]=[C:3]2/[CH:4]=[CH:5][C:6](=[O:8])[O:7]/2)=[CH:12][CH:11]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 5
実験手順
A mixture containing 5-bromomethylene-2(5H)furanone (0.175 g, 1 mmol), 4-fluorophenylboronic acid (0.168 g, 1.2 mmol), trans-dichlorobis(triphenylphosphine)palladium (II) (0.035 g, 0.05 mmol), tetrabutylammonium iodide (0.018 g, 0.05 mmol) and cesium fluoride (0.456 g, 3 mmol) in toluene (10 mL) and water (10 mL) were stirred at reflux for 24 hours under nitrogen. After cooling, brine (50 mL) was added and the product extracted with ethyl acetate (50 mL×3). The organic fractions were combined, washed with brine (50 mL×3), dried over anhydrous sodium sulfate and evaporated to dryness to give a brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum) giving the desired product 28 as a white powder. Yield 0.164 g (86%), m.p. 140-142° C., UV-Vis λmax (MeOH) 225(22535), 330(56424) nm.
後処理
- temperatureat reflux for 24 hours under nitrogen
- temperatureAfter cooling
- extractionthe product extracted with ethyl acetate (50 mL×3)
- washwashed with brine (50 mL×3)
- dry with materialdried over anhydrous sodium sulfate
- customevaporated to dryness
- customto give a brown solid
- customThe resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum)
出典と根拠
- ORDレコード
- ord-c05c6a584da64c3590114767d6827ae3
- 出典データセット
- uspto-grants-2013_11
- 特許番号
- US08586618B2
反応ノート
読み込み中…