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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427108Generated: November 3, 2026

Water → 4-bromo-5-chloro-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carbaldehyde

https://huagongshe.com/reaction/2427108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorosuccinimideHCID 31398—
Reactant4-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carbaldehydeHCID 86632547—
SolventTetrahydrofuranHCID 8028—
Product4-bromo-5-chloro-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carbaldehydeHCID 8663256174.4%

Reaction Steps

To a solution of 3.0 g of 3-chloro-2-(4-bromo-2-formyl-1H-pyrrol-1-yl)-pyridine in 30 ml of tetrahydrofuran was added 1.5 g of N-chlorosuccinimide. The resulting mixture was stirred at room temperature for 2 days. Water was poured into the reaction mixture, and the mixture was extracted with ethyl acetate two times. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 2.5 g of 4-bromo-5-chloro-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carbaldehyde of the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968573B2
Source datasetuspto-grants-2011_06
ORD IDord-b779c2e683e247ccaa0a472317b55430
Source noteuspto-grants-2011_06