Ethyl 5-bromo-4-(p-chlorophenyl)pyrrole-3-carboxylate → 5-Bromo-4-(p-chlorophenyl)pyrrole-3-carboxylic acid

HRID 1085611Notes

Reaction equation

HRID 1085611 reaction equation
[Br:1][C:2]1[NH:6][CH:5]=[C:4]([C:7]([O:9]CC)=[O:8])[C:3]=1[C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][CH:13]=1>[OH-].[Na+]>[Br:1][C:2]1[NH:6][CH:5]=[C:4]([C:7]([OH:9])=[O:8])[C:3]=1[C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][CH:13]=1

Participants

3

Reactant 1

HCID 15010185Ethyl 5-bromo-4-(p-chlorophenyl)pyrrole-3-carboxylate

Product 1

HCID 157530185-Bromo-4-(p-chlorophenyl)pyrrole-3-carboxylic acid

Reagents, catalysts & solvents 1

HCID 14798Sodium HydroxideSolvent

Procedure

Ethyl 5-bromo-4-(p-chlorophenyl)pyrrole-3-carboxylate (15 g., 0.045 mmol) is added to 200 mL of 10% sodium hydroxide and the slurry heated to reflux. After everything appears to dissolve the mixture is refluxed an additional 40 minutes. The mixture is cooled, filtered and the filtrate acidified. The white precipitate (8.0 g, 58%) is collected and dried. The solid has m.p. >205° C. and an NMR (d6 -DMSO) which showed a pyrrole proton at 7.52 (d). The mass spectrum is also consistent for a monobrominated compound.

Workup

  1. temperaturethe slurry heated to reflux
  2. dissolutionto dissolve the mixture
  3. temperatureis refluxed an additional 40 minutes
  4. temperatureThe mixture is cooled
  5. filtrationfiltered
  6. customThe white precipitate (8.0 g, 58%) is collected
  7. customdried

Sources & evidence

ORD record
ord-d04f56ed83d7470fb8982b7ad4ed849c
Source dataset
uspto-grants-1991_04
Patent number
US05010098

Reaction notes

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