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Acetyl chloride → 3'-Acetylaminomethylacetophenone

HRID 1734012
ノート
印刷プレビュー

反応式

HRID 1734012 の反応式
[C:1](Cl)(=[O:3])[CH3:2].Cl.[C:6]([C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=1)[CH2:12][NH2:13])(=[O:8])[CH3:7].C(N(CC)CC)C>ClCCl>[C:1]([NH:13][CH2:12][C:11]1[CH:10]=[C:9]([C:6](=[O:8])[CH3:7])[CH:16]=[CH:15][CH:14]=1)(=[O:3])[CH3:2]
参加物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 6367Acetyl chlorideHCID 8471TriethylamineHCID 247213721-[3-(aminomethyl)phenyl]ethan-1-one hydrochloride

生成物 1

HCID 107977903'-Acetylaminomethylacetophenone収率 62.1%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

Acetyl chloride (2.5 g) was added slowly to a suspension of 3-acetylbenzylamine hydrochloride (5.0 g) and triethylamine (6.0 g) in dichloromethane (50 ml) with cooling on an ice-water bath. The mixture was stirred at room temperature for 10 hours. The solvent was removed under reduced pressure. The residue was dissolved in water (100 ml). The solution was alkalified with an aqueous potassium carbonate solution. The mixture was extracted with ethyl acetate (150 ml). The solution was dried with magnesium sulfate. The solvent was removed under reduced pressure to afford 3'-acetylaminomethylacetophenone (3.2 g) (oil).

後処理

  1. temperaturewith cooling on an ice-water bath
  2. customThe solvent was removed under reduced pressure
  3. dissolutionThe residue was dissolved in water (100 ml)
  4. extractionThe mixture was extracted with ethyl acetate (150 ml)
  5. dry with materialThe solution was dried with magnesium sulfate
  6. customThe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-2db5fdd751924e1eb61013a002d6db61
出典データセット
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05532258

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート