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Water → p-(3-Phthalimidopropoxy)acetophenone

HRID 1732485
ノート
印刷プレビュー

反応式

HRID 1732485 の反応式
Br[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12](=[O:14])[CH3:13])=[CH:8][CH:7]=1.[C:15]1(=[O:25])[NH:19][C:18](=[O:20])[C:17]2=[CH:21][CH:22]=[CH:23][CH:24]=[C:16]12.[K].O>CN(C)C=O>[C:15]1(=[O:25])[N:19]([CH2:2][CH2:3][CH2:4][O:5][C:6]2[CH:11]=[CH:10][C:9]([C:12](=[O:14])[CH3:13])=[CH:8][CH:7]=2)[C:18](=[O:20])[C:17]2=[CH:21][CH:22]=[CH:23][CH:24]=[C:16]12
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 10061000HCID 10061000、化合物HCID 24194345Phthalimide potassium salt

生成物 1

HCID 20306529p-(3-Phthalimidopropoxy)acetophenone収率 89%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
70 °C

実験手順

p-(3-Bromopropoxy)acetophenone (5.14 g.) and potassium phthalimide (3.75 g.) were dissolved in anhydrous N,N-dimethylformamide (50 ml.), and the solution was stirred at 70° C. for 2.5 hours. After the reaction mixture was allowed to cool, water (300 ml.) was poured thereto. The aqueous solution was extracted three times with ethyl acetate, and the extract was washed with ethyl acetate and then dried over magnesium sulfate. The ethyl acetate was removed by evaporation from the solution under reduced pressure, and the resultant residue was treated with ether to give p-(3-phthalimidopropoxy)acetophenone (5.75 g.).

後処理

  1. temperatureto cool
  2. extractionThe aqueous solution was extracted three times with ethyl acetate
  3. washthe extract was washed with ethyl acetate
  4. dry with materialdried over magnesium sulfate
  5. customThe ethyl acetate was removed by evaporation from the solution under reduced pressure
  6. additionthe resultant residue was treated with ether

出典と根拠

ORDレコード
ord-e8ec19c11ea14c5ba6aa433bde0f7a3d
出典データセット
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04237305

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート