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Hydrochloric Acid → HCID 68831193、化合物

HRID 747709
ノート
印刷プレビュー

反応式

HRID 747709 の反応式
Cl[CH2:2][CH2:3][CH2:4][CH2:5][C:6]([C:8]1[CH:15]=[CH:14][C:11]([C:12]#[N:13])=[CH:10][CH:9]=1)=[O:7].C(=O)([O-])[O-].[K+].[K+].[I-].[K+].[OH:24][C:25]1[CH:26]=[C:27]([CH:30]=[CH:31][CH:32]=1)[C:28]#[N:29].Cl>CN(C)C=O>[C:12]([C:11]1[CH:14]=[CH:15][C:8]([C:6](=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2][O:24][C:25]2[CH:26]=[C:27]([CH:30]=[CH:31][CH:32]=2)[C:28]#[N:29])=[CH:9][CH:10]=1)#[N:13]
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

7

反応物 5

HCID 313Hydrochloric AcidHCID 4875Potassium IodideHCID 11430Potassium CarbonateHCID 133943-CyanophenolHCID 177891304-(5-Chloropentanoyl)benzonitrile

生成物 1

HCID 68831193HCID 68831193、化合物

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

反応条件

温度
70 °C

実験手順

53 mg (0.24 mmol) of 4-(5-chloro-1-oxopentyl)benzonitrile was dissolved in 2 ml of dimethylformamide. 33 mg (0.24 mmol) of potassium carbonate, 40 mg of potassium iodide and 29 mg (0.24 mmol) of 3-hydroxybenzonitrile were added to the solution, and they were stirred at 70° C. overnight. 1 N Hydrochloric acid was added to the reaction mixture. After the extraction with ethyl acetate, the extract was washed with 1 N aqueous sodium hydroxide solution and saturated aqueous common salt solution, and then dried over powdery magnesium sulfate. The solvent was evaporated, and the residue was purified by the silica gel chromatography to obtain the title compound.

後処理

  1. extractionAfter the extraction with ethyl acetate
  2. washthe extract was washed with 1 N aqueous sodium hydroxide solution and saturated aqueous common salt solution
  3. dry with materialdried over powdery magnesium sulfate
  4. customThe solvent was evaporated
  5. customthe residue was purified by the silica gel chromatography

出典と根拠

ORDレコード
ord-2b5e7c2bcbae490aa06a6c5fe28e967c
出典データセット
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07396844B1

反応ノート

読み込み中…

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