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Hydrochloric Acid → 4-(4-(ethoxycarbonyl)-5-methyl-1H-pyrrol-3-yl)butanoic acid

HRID 626867
Notes
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Reaction equation

HRID 626867 reaction equation
Cl.[NH2:2][CH2:3][C:4](=O)[CH2:5][CH2:6][CH2:7][C:8]([OH:10])=[O:9].[C:12]([O:18][CH2:19][CH3:20])(=[O:17])[CH2:13][C:14]([CH3:16])=O.C(O[Na])(C)=O.Cl>O>[CH2:19]([O:18][C:12]([C:13]1[C:4]([CH2:5][CH2:6][CH2:7][C:8]([OH:10])=[O:9])=[CH:3][NH:2][C:14]=1[CH3:16])=[O:17])[CH3:20]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 8868Ethyl AcetoacetateHCID 713866726-Amino-5-oxohexanoic acid hydrochlorideHCID 178418247HCID 178418247, compound

Product 1

HCID 593760204-(4-(ethoxycarbonyl)-5-methyl-1H-pyrrol-3-yl)butanoic acidYield 70.6%

Reagents, catalysts & solvents 1

HCID 962
Water
Solvent

Procedure

6-amino-5-oxohexanoic acid hydrochloride (9.73 g, 49.8 mmol) was dissolved in H2O (35 mL), and ethyl acetoacetate (5.51 g, 42.34 mmol) and AcONa (20.3 g, 14.95 mmol) were added to the above-mentioned solution. The reaction solution was refluxed for 1 h, cooled to room temperature and 0.5N HCl was added until a pH of about 5 was reached. The combined organic layers were anidrified on Na2SO4, filtered and concentred to give 7.15 g (yield: 60%) of the title compound as brown solid.

Workup

  1. temperatureThe reaction solution was refluxed for 1 h
  2. filtrationfiltered

Sources & evidence

ORD record
ord-209d1b12ce804050b566858eb3cf9138
Source dataset
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09309253B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes