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Potassium Hydroxide → 3-Acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid

HRID 917796
ノート
印刷プレビュー

反応式

HRID 917796 の反応式
C([O:3][C:4]([C:6]1[NH:7][C:8]([CH3:15])=[C:9]([CH3:14])[C:10]=1[C:11](=[O:13])[CH3:12])=[O:5])C.[OH-].[K+]>C(O)C>[C:11]([C:10]1[C:9]([CH3:14])=[C:8]([CH3:15])[NH:7][C:6]=1[C:4]([OH:5])=[O:3])(=[O:13])[CH3:12]
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 14797Potassium HydroxideHCID 12288399Ethyl 3-acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylate

生成物 1

HCID 5906793-Acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid収率 81.7%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A mixture of pyrrole ester 9b (8.2 g, 0.0392 mol), in ethanol and 100 mL of 10% potassium hydroxide were refluxed for 1 h. The mixture was cooled and concentrated in vacuo to an oil. Water was added to the oil, the mixture acidified with dilute HCl and extracted with ether. The organic phase was dried with anhy. sodium sulfate and concentrated in vacuo to a solid residue. The compound was recrystallized in 80 mL of ethanol to give 5.8 g of pure 3-acetyl-4,5-dimethyl-2-pyrrole carboxylic acid 10b as a solid.

後処理

  1. temperatureThe mixture was cooled
  2. concentrationconcentrated in vacuo to an oil
  3. additionWater was added to the oil
  4. extractionextracted with ether
  5. customThe organic phase was dried with anhy
  6. concentrationsodium sulfate and concentrated in vacuo to a solid residue
  7. customThe compound was recrystallized in 80 mL of ethanol

出典と根拠

ORDレコード
ord-b0aace673b2641c2ae547b7de139cd09
出典データセット
uspto-grants-2007_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07273885B2

反応ノート

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