Ethyl Acetate → 6-(4,5-Methylenedioxy-2-nitrophenyl)-2,3-dimethoxynaphthalene
反応式
C[Sn](C)(C)[C:3]1[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][C:6]2[O:12][CH2:13][O:14][C:5]=2[CH:4]=1.[C:17]([O:20][CH2:21][CH3:22])(=O)C>C1COCC1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH2:13]1[O:14][C:5]2[C:6](=[CH:7][C:8]([N+:9]([O-:11])=[O:10])=[C:3]([C:3]3[CH:4]=[C:5]4[C:6](=[CH:7][CH:8]=3)[CH:22]=[C:21]([O:20][CH3:17])[C:21]([O:20][CH3:17])=[CH:22]4)[CH:4]=2)[O:12]1参加物
実験手順
Tetrakis(triphenylphosphine)palladium(0) (40 mg) and cuprous bromide (8 mg) were added to a solution of 6,7-dimethoxy-2-naphthalenetriflate (160 mg, 0.48 mmol) and trimethyl(3,4-methylenedioxy-6-nitrophenyl)stannane (8, 187 mg, 0.57 mmol) in THF (20 mL). The mixture was stirred at room temperature for 0.5 h., and then refluxed under nitrogen for 18 h. After Cooling, THF was rotaevaporated and ethyl acetate (50 ml) was added to the residue. the solution was washed with water (30 mL). The organic layer was separated and passed through a celite bed to remove suspended particles. The organic layer was then washed with brine, dried (anhydrous Na2SO4) and concentrated in vacuo. The residue was chromatographed on silica gel using 70:30 hexanes:ethyl acetate to give a mixture of two compounds with same Rf value. The mixture can be separated after the hydrogenation step.
後処理
- temperaturerefluxed under nitrogen for 18 h
- temperatureAfter Cooling
- washthe solution was washed with water (30 mL)
- customThe organic layer was separated
- customto remove
- washThe organic layer was then washed with brine
- dry with materialdried (anhydrous Na2SO4)
- concentrationconcentrated in vacuo
- customThe residue was chromatographed on silica gel using 70:30 hexanes
- customethyl acetate to give
- additiona mixture of two compounds with same Rf value
- customThe mixture can be separated after the hydrogenation step
出典と根拠
- ORDレコード
- ord-706b38464bbe458c9fb13de40f8d4ea8
- 出典データセット
- uspto-grants-2004_05
- 特許番号
- US06740650B2
反応ノート
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