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Ethyl cyanoacetate → 2-cyano-N-[3-(dimethylamino)propyl]acetamide

HRID 1067870
ノート
印刷プレビュー

反応式

HRID 1067870 の反応式
[C:1]([CH2:3][C:4]([O:6]CC)=O)#[N:2].[CH3:9][N:10]([CH3:15])[CH2:11][CH2:12][CH2:13][NH2:14]>C1(C)C=CC=CC=1>[C:1]([CH2:3][C:4]([NH:14][CH2:13][CH2:12][CH2:11][N:10]([CH3:15])[CH3:9])=[O:6])#[N:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 7764Ethyl cyanoacetateHCID 7993N,N-Dimethyl-1,3-propanediamine

生成物 1

HCID 50583022-cyano-N-[3-(dimethylamino)propyl]acetamide収率 96%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

Ethyl cyanoacetate (51.106 g, 0.4518 mole) was added to 3-(dimethylamino) propylamine (46.162 g, 0.4518 mole) in a 250 ml round bottom flask equipped with a magnetic stir bar. After stirring for approximately 0.5 hr, 50 ml of toluene was added. The clear orange liquid was stirred at room temperature for approximately 15 hours, after which the ethanol and toluene were removed via vacuum distillation. 2-Cyano-N-[3-(dimethylamino)propyl]acetamide was obtained in 96% yield.

後処理

  1. customequipped with a magnetic stir bar
  2. stirringThe clear orange liquid was stirred at room temperature for approximately 15 hours
  3. customafter which the ethanol and toluene were removed via vacuum distillation

出典と根拠

ORDレコード
ord-433b1c351aab4497821ec99175586d5b
出典データセット
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06248801B1

反応ノート

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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