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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251997Generated: October 28, 2026

Acetone → 4-bromo-1-(3-chloro-4-pyridinyl)-1H-pyrrole-2-carboxylic acid

https://huagongshe.com/reaction/251997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium HydroxideHCID 14798—
ReactantPotassium PermanganateHCID 516875—
Reactant4-bromo-1-(3-chloro-4-pyridinyl)-1H-pyrrole-2-carbaldehydeHCID 86632560—
SolventWaterHCID 962—
Product4-bromo-1-(3-chloro-4-pyridinyl)-1H-pyrrole-2-carboxylic acidHCID 66853912—

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of 2.0 g of potassium permanganate in 10 ml of water was added dropwise to a mixture of 1.2 g of 4-bromo-1-(3-chloro-4-pyridinyl)-1H-pyrrole-2-carbaldehyde and 30 ml of acetone while the mixture was maintained at 40° C. The resulting mixture was stirred at 60° C. for 1 hour. A precipitate was 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, and then extracted with ethyl acetate two times. The organic layers were combined, washed successively with water and an aqueous saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain 0.43 g of 4-bromo-1-(3-chloro-4-pyridinyl)-1H-pyrrole-2-carboxylic acid of the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07867949B2
Source datasetuspto-grants-2011_01
ORD IDord-9af5ef2086134ed7b5cde731def3548f
Source noteuspto-grants-2011_01