反应方程式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9](=O)[CH2:10]C)=[CH:5][CH:4]=1.C[C:14]([O-:16])=[O:15].CC([O-])=O.CC([O-])=O.CC([O-])=O.[Pb+2].C(OC(OCC)OCC)C.Cl(O)(=O)(=O)=O>[OH-].[K+].O.CO>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH:9]([CH3:10])[C:14]([OH:16])=[O:15])=[CH:7][CH:8]=1参与物
反应条件
- 温度
- 55 °C
实验过程
A mixture of p-methoxypropiophenone (2.39 g, 14.5 mmol), 90% lead(IV)acetate (6.45 g, 14.5 mmol), triethylorthoformate (15 ml) and 70% perchloric acid (1.2 ml. 29 mmol) was heated to 55° C. for 18 h. The mixture was cooled and the triethylorthoformate removed under reduced pressure. The residue was dissolved in CHCl3 and the remaining precipitate filtered off and discarded. The CHCl3 solution was then washed with water and evaporated to yield the crude ester. This crude ester product was dissolved in a 10% KOH 1:1 water:methanol solution, which was then refluxed for 3 h. After cooling the methanol was evaporated under reduced pressure and the aqueous solution washed with diethylether (3×25 ml). The aqueous solution was acidified with 2N H2SO4, then washed again with diethylether (3×25 ml). The combined fractions from the second ether wash were dried (Na2SO4) and evaporated to give the propionic acid (1.66 g, 63%).
后处理
- temperatureThe mixture was cooled
- customthe triethylorthoformate removed under reduced pressure
- dissolutionThe residue was dissolved in CHCl3
- filtrationthe remaining precipitate filtered off
- washThe CHCl3 solution was then washed with water
- customevaporated
- customto yield the crude ester
- customwas evaporated under reduced pressure
- washthe aqueous solution washed with diethylether (3×25 ml)
- washwashed again with diethylether (3×25 ml)
- washThe combined fractions from the second ether wash
- dry with materialwere dried (Na2SO4)
- customevaporated
来源与证据
- ORD记录
- ord-99151606da9146d283d898a9af3d839d
- 来源数据集
- uspto-grants-2003_11
- 专利号
- US06649648B1
关联笔记
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