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Hydrochloric Acid → 4-Propionamidocinnamic acid

HRID 726292
ノート
印刷プレビュー

反応式

HRID 726292 の反応式
[C:1]([NH:5][C:6]1[CH:18]=[CH:17][C:9]([CH:10]=[CH:11][C:12]([O:14]CC)=[O:13])=[CH:8][CH:7]=1)(=[O:4])[CH2:2][CH3:3].[OH-].[Na+].Cl>C(O)C>[C:1]([NH:5][C:6]1[CH:18]=[CH:17][C:9]([CH:10]=[CH:11][C:12]([OH:14])=[O:13])=[CH:8][CH:7]=1)(=[O:4])[CH2:2][CH3:3]
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 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 54078953Ethyl 4-propionamidocinnamate

生成物 1

HCID 538191414-Propionamidocinnamic acid収率 81.1%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of ethyl 4-propionamidocinnamate (160 mg) in ethanol (5 ml) was added 1N aqueous sodium hydroxide solution (1.5 ml) at ambient temperature. The mixture was stirred at same temperature for 14 hours, and then at 40° C. for 2 hours. 1N-hydrochloric acid (1.5 ml) was added to the reaction mixture and evaporated in vacuo. The residue was diluted with 10% methanol-dichloromethane, washed with water, dried over magnesium sulfate and evaporated in vacuo. The residue was crystallized from diisopropyl ether to give 4-propionamidocinnamic acid (115 mg) as a colorless powder.

後処理

  1. waitat 40° C. for 2 hours
  2. customevaporated in vacuo
  3. additionThe residue was diluted with 10% methanol-dichloromethane
  4. washwashed with water
  5. dry with materialdried over magnesium sulfate
  6. customevaporated in vacuo
  7. customThe residue was crystallized from diisopropyl ether

出典と根拠

ORDレコード
ord-1daf3791ecb743b3899e9a0bd337e659
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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