Potassium Iodide → 1-(2-Methoxyphenyl)-1-[4-(3-phenylpropoxy)-phenyl]-propan-1-ol

HRID 364776ノート

反応式

HRID 364776 の反応式
[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

  1. temperatureAfter cooling
  2. distillationacetone is distilled off under reduced pressure, to the residue water
  3. additionis added
  4. extractionit is extracted with benzene
  5. washThe organic phase is washed to neutral with water
  6. dry with materialAfter drying over anhydrous magnesium sulfate the solution
  7. customis evaporated in vacuo
  8. customThe residue is crystallized from n-hexane
  9. 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…