HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 5-bromo-4-(p-chlorophenyl)pyrrole-3-carboxylate → 5-Bromo-4-(p-chlorophenyl)pyrrole-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 5-bromo-4-(p-chlorophenyl)pyrrole-3-carboxylate | HCID 15010185 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 5-Bromo-4-(p-chlorophenyl)pyrrole-3-carboxylic acid | HCID 15753018 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04929634 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-5ea6f256c41a4fb8b03160d44716d72a |
| Source note | uspto-grants-1990_05 |