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Dimethylformamide → Ethyl 5-formyl-4-methyl-1H-pyrrole-2-carboxylate

HRID 983048
ノート
印刷プレビュー

反応式

HRID 983048 の反応式
P(Cl)(Cl)(Cl)=O.[CH2:6]([O:8][C:9]([C:11]1[NH:12][CH:13]=[C:14]([CH3:16])[CH:15]=1)=[O:10])[CH3:7].[OH-].[Na+].CN(C)[CH:21]=[O:22]>O>[CH2:6]([O:8][C:9]([C:11]1[NH:12][C:13]([CH:21]=[O:22])=[C:14]([CH3:16])[CH:15]=1)=[O:10])[CH3:7]
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 4

HCID 6228Dimethylformamide2 回HCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 643361Ethyl 4-methyl-1H-pyrrole-2-carboxylate

生成物 1

HCID 9855648Ethyl 5-formyl-4-methyl-1H-pyrrole-2-carboxylate収率 68%

試薬・触媒・溶媒 1

HCID 962
Water
溶媒

実験手順

To the ice-cold 3 mL (39.2 mmol) of dimethylformamide (DMF) was added phosphorus oxychloride (0.67 mL, 7.18 mmol) drop wise and the resultant mixture was stirred for 30 minutes. A solution of 1 g (6.53 mmol) of 4-methyl-1H-pyrrole-2-carboxylic acid ethyl ester in 3 mL of DMF was added to the reaction. After 1 h, the reaction was warmed to room temperature for another 2.5 h. The reaction mixture was diluted with water (100 mL) and basified to pH=11 with 1N sodium hydroxide solution. The precipitate was removed by filtration, rinsing with water and dried to afford 0.8 g (68%) of 5-formyl-4-methyl-1H-pyrrole-2-carboxylic acid ethyl ester as a white solid.

後処理

  1. customThe precipitate was removed by filtration
  2. washrinsing with water
  3. customdried

出典と根拠

ORDレコード
ord-8d5f6345d7944baab5693ccdc0b0558d
出典データセット
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06861418B2

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