HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427052Generated: November 1, 2026
Acetone → 4-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxylic acid
https://huagongshe.com/reaction/2427052
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 4-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carbaldehyde | HCID 86632547 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxylic acid | HCID 66854487 | — |
Reaction Steps
An aqueous solution of 1.2 g of potassium permanganate in 10 ml of water was added dropwise to a mixture of 0.72 g of 4-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carbaldehyde and 15 ml of acetone while the mixture was retained at 40° C. The mixture was then stirred at 60° C. for 8 hours. Precipitates were filtered off to obtain a filtrate. The filtrate was adjusted to pH 10-12 by an addition of a 2N aqueous sodium hydroxide solution, and then washed with chloroform two times. The aqueous layer was adjusted to around pH 3 by an addition of 2N hydrochloric acid. A deposited precipitate was collected by filtration to obtain 0.56 g of 4-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxylic acid of the formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968573B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-58dd30f12aa54ec78fe245e8d7e26051 |
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| Source note | uspto-grants-2011_06 |
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