HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251963Generated: October 29, 2026
Acetone → 4,5-dibromo-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxylic acid
https://huagongshe.com/reaction/251963
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | HCID 86632550 | HCID 86632550 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4,5-dibromo-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxylic acid | HCID 66854245 | — |
Reaction Steps
To a mixture of 1.0 g of 4,5-dibromo-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carbaldehyde, 15 ml of acetone and 7 ml of water was slowly added 1.3 g of potassium permanganate at 40° C. The resulting mixture was stirred at 60° C. for 2 hours. Precipitates in the reaction mixture were removed by filtration. The resulting filtrate was washed with chloroform two times. The aqueous layer was adjusted to around pH 3 by an addition of 2N hydrochloric acid and then extracted with ethyl acetate three times. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure to obtain 0.69 g of 4,5-dibromo-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxylic acid of the formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07867949B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-d230ad2275694666b3c5b697ba7d4dea |
|---|
| Source note | uspto-grants-2011_01 |
|---|