Potassium Iodide → 1-(2-Methoxyphenyl)-1-[4-(3-phenylpropoxy)-phenyl]-propan-1-ol
反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]([C:13]1[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][CH:14]=1)([OH:12])[CH2:10][CH3:11].[C:20]1([CH2:26][CH2:27][CH2:28]Br)[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.C(=O)([O-])[O-].[K+].[K+].[I-].[K+]>CC(C)=O>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]([C:13]1[CH:18]=[CH:17][C:16]([O:19][CH2:28][CH2:27][CH2:26][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[CH:15][CH:14]=1)([OH:12])[CH2:10][CH3:11]参加物
6
実験手順
6.45 g. of 1-(2-methoxyphenyl)-1-(4-hydroxyphenyl)-propan-1-ol, 5.5 g. of 3-phenylpropyl bromide, 6.5 g. of anhydrous potassium carbonate, 0.5 g. of potassium iodide and 65 ml. of dry acetone are slightly boiled for 15 hours, with stirring. After cooling, acetone is distilled off under reduced pressure, to the residue water is added and it is extracted with benzene. The organic phase is washed to neutral with water, a 5% aqueous sodium hydroxide solution and again water. After drying over anhydrous magnesium sulfate the solution is evaporated in vacuo. The residue is crystallized from n-hexane to yield 7.8 g. of the named compound, melting at 75°-76° C.
後処理
- temperatureAfter cooling
- distillationacetone is distilled off under reduced pressure, to the residue water
- additionis added
- extractionit is extracted with benzene
- washThe organic phase is washed to neutral with water
- dry with materialAfter drying over anhydrous magnesium sulfate the solution
- customis evaporated in vacuo
- customThe residue is crystallized from n-hexane
- customto yield 7.8 g
出典と根拠
- ORDレコード
- ord-9e3d53cde45f433ba65cd38e51d2cc18
- 出典データセット
- uspto-grants-1986_08
- 特許番号
- US04605785
反応ノート
読み込み中…