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Ethanolamine → 1,2-Dimethyl-4-phenyl-1H-pyrrole

HRID 880437
ノート
印刷プレビュー

反応式

HRID 880437 の反応式
[CH3:1][N:2]1[C:6]([CH3:7])=[C:5](C(O)=O)[C:4]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[C:3]1C(O)=O.NCCO>O>[CH3:1][N:2]1[CH:3]=[C:4]([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:5]=[C:6]1[CH3:7]
参加物反応条件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 700EthanolamineHCID 669150311,5-dimethyl-3-phenyl-1H-pyrrole-2,4-dicarboxylic acid

生成物 1

HCID 447182881,2-Dimethyl-4-phenyl-1H-pyrrole収率 78%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
175 °C

実験手順

A suspension of 1,5-dimethyl-3-phenyl-pyrrole-2,4-dicarboxylic acid (60 g, 0.23 mol) and 2-aminoethanol (300 mL) was heated to 175° C. under a nitrogen atmosphere for 30 min. The mixture was allowed to cool to room temperature, diluted with water (100 mL) and extracted with ethyl acetate (2×100 mL). The combined organic layers were washed successively with water (3×100 mL) and brine (2×100 mL), dried over anhydrous sodium sulfate and concentrated in vacuo at a temperature below 40° C. to afford the crude product. Flash column chromatography over neutral alumina using 5% ethyl acetate in petroleum ether as eluent afforded 1,2-dimethyl-4-phenyl-pyrrole (30.5 g, 78%) as a white solid.

後処理

  1. temperatureto cool to room temperature
  2. extractionextracted with ethyl acetate (2×100 mL)
  3. washThe combined organic layers were washed successively with water (3×100 mL) and brine (2×100 mL)
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo at a temperature below 40° C.
  6. customto afford the crude product

出典と根拠

ORDレコード
ord-16bfd1830fb840d4b93c119aed111638
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08993574B2

反応ノート

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