Benzoic Acid → N,N-Diethylbenzamide

HRID 638775

反応式

HRID 638775 の反応式
S(Cl)(Cl)=O.[C:5]([OH:13])(=O)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[CH2:14]([NH:16][CH2:17][CH3:18])[CH3:15]>O>[CH2:14]([N:16]([CH2:17][CH3:18])[C:5](=[O:13])[C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1)[CH3:15]

参加物

5

反応条件

温度
-10 °C

実験手順

A mixture of thionyl chloride (6 mL) and the benzoic acid was heated at reflux until the starting benzoic acid dissolved. Excess thionyl chloride was removed under reduced pressure leaving the crude acid chloride as a low melting solid which was used without further purification. The crude acid chloride was dissolved in CH2Cl2 (20 mL) and cooled to −10° C. To this stirred solution was added triethylamine (4 mL), followed by the dropwise addition of diethylamine (1.4 equivalents). The heterogeneous reaction mixture was allowed to warm to room temperature and was stirred for 30 minutes. The reaction mixture was transferred to a separatory funnel containing H2O (20 mL). The organic layer was separated and washed with 5% HCl (2×25 mL), H2O (25 ml), and dried over Na2SO4. The solvent was removed under reduced pressure to afford the product N,N-diethyl benzamide.

後処理

  1. dissolutiondissolved
  2. customExcess thionyl chloride was removed under reduced pressure
  3. customleaving the crude acid chloride as a low melting solid which
  4. customwas used without further purification
  5. dissolutionThe crude acid chloride was dissolved in CH2Cl2 (20 mL)
  6. additionTo this stirred solution was added triethylamine (4 mL)
  7. temperatureto warm to room temperature
  8. customThe reaction mixture was transferred to a separatory funnel
  9. customThe organic layer was separated
  10. washwashed with 5% HCl (2×25 mL), H2O (25 ml)
  11. dry with materialdried over Na2SO4
  12. customThe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-6c0dfa1e9b384a449dcd9516980e7d72
出典データセット
uspto-grants-2010_04
特許番号
US07691494B2

関連ノート

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