HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888974Generated: October 31, 2026
Potassium Hydroxide → 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic Acid
https://huagongshe.com/reaction/1888974
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | ethyl 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylate | HCID 137485 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic Acid | HCID 11073792 | — |
Reaction Steps
Into a 10-L four necked round-bottomed flask equipped with a mechanical stirrer, a thermometer pocket, addition funnel and reflux condenser were charged 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid ethyl ester (IV) (0.6 Kg; 3.09 mole), methanol (2.0 L) and aqueous KOH solution (prepared by dissolving 450 g KOH in 1.8 L of water), stirred well and raised the reaction mass temperature to 60-70° C. and maintained for 4-6 hours. The progress of the reaction was monitored by TLC. After completion of the reaction, the excess solvent was removed under diminished pressure and the resulting product was diluted with water and extracted with ethylacetate. The aqueous layer was separated and the pH adjusted to 4.0 with conc. HCl. The resulting solution was stirred over night at 25-30° C. The product was filtered and washed with water. The product was dried at 60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501962B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-a0265f6edfee48d98ad9476bb09e138a |
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| Source note | uspto-grants-2013_08 |
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