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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088964Generated: October 31, 2026

Acetyl chloride → 1-(5-bromo-1H-pyrrolo[2,3-b]pyridin-3-yl)ethanone

https://huagongshe.com/reaction/2088964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
SolventDichloromethaneHCID 6344—
Product1-(5-bromo-1H-pyrrolo[2,3-b]pyridin-3-yl)ethanoneHCID 59699914—

Reaction Steps

Aluminum trichloride (846 mg) was added to a solution of 5-bromo-1H-pyrrolo[2,3-b]pyridine (250 mg) in dichloromethane (5 ml) at room temperature over 10 minutes. Subsequently, acetyl chloride (135 μl) was added and the mixture was stirred at room temperature for 5 hours. The reaction solution was poured into ice-cold water and separated by adding dichloromethane. The resulting organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (developed with methanol-chloroform) to give the title compound (186 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436012B2
Source datasetuspto-grants-2013_05
ORD IDord-1e8bd49c81934c67ad6b362709931e9a
Source noteuspto-grants-2013_05