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Ethanol → 5-(2-carboxy-ethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester

HRID 1072191
ノート
印刷プレビュー

反応式

HRID 1072191 の反応式
[OH-].[Li+].[CH2:3]([O:5][C:6]([C:8]1[NH:9][C:10]([CH2:14][CH2:15][C:16]([O:18]C(C)(C)C)=[O:17])=[CH:11][C:12]=1[CH3:13])=[O:7])[CH3:4].C(O)C>CO.O>[CH2:3]([O:5][C:6]([C:8]1[NH:9][C:10]([CH2:14][CH2:15][C:16]([OH:18])=[O:17])=[CH:11][C:12]=1[CH3:13])=[O:7])[CH3:4]
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 702EthanolHCID 3939Lithium HydroxideHCID 697094735-(2-tert-butoxycarbonyl-ethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester

生成物 1

HCID 697080675-(2-carboxy-ethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester収率 98.4%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒
HCID 962
Water
溶媒
2 回

実験手順

Lithium hydroxide (1.02 g, 42.65 mmol) was added to a suspension of 5-(2-tert-butoxycarbonyl-ethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester (2.4 g, 8.53 mmol) in methanol (50 mL) and water (12 mL). Ethanol (4 mL) was added to the mixture (to aid solvation of the starting material) and it was stirred at room temperature for overnight. The reaction was diluted with water (20 mL), concentrated (to remove most of the alcohol) and extracted with ether. The aqueous layer was the acidified to pH=2 using 1N HCl (43 mL) and extracted with ethyl acetate (2×). The combined extract was then washed with brine, dried and concentrated to give 1.89 g of 5-(2-carboxy-ethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester as a white solid.

後処理

  1. concentrationconcentrated (
  2. customto remove most of the alcohol) and
  3. extractionextracted with ether
  4. extractionextracted with ethyl acetate (2×)
  5. extractionThe combined extract
  6. washwas then washed with brine
  7. customdried
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-7274da72199f439c9be70c3f112a779d
出典データセット
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06908930B2

反応ノート

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