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Triethylamine → Ethyl 4-propionamidocinnamate

HRID 726287
ノート
印刷プレビュー

反応式

HRID 726287 の反応式
[NH2:1][C:2]1[CH:14]=[CH:13][C:5]([CH:6]=[CH:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])=[CH:4][CH:3]=1.C(N(CC)CC)C.[C:22](Cl)(=[O:25])[CH2:23][CH3:24]>ClCCl.CN(C)C(N)CC>[C:22]([NH:1][C:2]1[CH:3]=[CH:4][C:5]([CH:6]=[CH:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])=[CH:13][CH:14]=1)(=[O:25])[CH2:23][CH3:24]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 8471TriethylamineHCID 62324Propionyl chlorideHCID 97826Ethyl 3-(4-aminophenyl)acrylate

生成物 1

HCID 54078953Ethyl 4-propionamidocinnamate収率 87.9%

試薬・触媒・溶媒 2

HCID 169191N,N-Dimethylpropanediamine触媒HCID 6344Dichloromethane溶媒2 回

実験手順

To a mixture of ethyl 4-aminocinnamate (300 mg), triethylamine (167 mg) and dichloromethane (3 ml) was added a solution of propionyl chloride (182 mg) in dichloromethane (1 ml) in an ice-water bath, and the mixture was stirred for 1 hour at the same temperature. To the reaction mixture was added 4 drops of N,N-dimethylpropanediamine, and the mixture was further stirred for 5 minutes. The reaction mixture was washed with water, dried over magnesium sulfate, and evaporated in vacuo. The residue was crystallized from diisopropyl ether to give ethyl 4-propionamidocinnamate (341 mg) as a colorless powder.

後処理

  1. stirringthe mixture was further stirred for 5 minutes
  2. washThe reaction mixture was washed with water
  3. dry with materialdried over magnesium sulfate
  4. customevaporated in vacuo
  5. customThe residue was crystallized from diisopropyl ether

出典と根拠

ORDレコード
ord-3e6d437ede3745ec89616b79efc77a12
出典データセット
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05708173

反応ノート

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