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

HRID 1072191
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HRID 1072191 반응식
[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]
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참가 물질

6

반응물 3

HCID 702EthanolHCID 3939Lithium HydroxideHCID 697094735-(2-tert-butoxycarbonyl-ethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester

생성물 1

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

시약·촉매·용매 2

HCID 887Methanol용매
HCID 962
Water
용매
2회

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-7274da72199f439c9be70c3f112a779d
출처 데이터셋
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06908930B2

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