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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479494Generated: October 25, 2026

m-Chloroperbenzoic acid → 5-Bromo-2-chloro-1-oxo-1lambda~5~-pyridine

https://huagongshe.com/reaction/1479494

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant5-Bromo-2-chloropyridineHCID 2734414—
SolventChloroformHCID 6212—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-2-chloro-1-oxo-1lambda~5~-pyridineHCID 16218324—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 5-bromo-2-chloropyridine (1.0 eq.) in chloroform (0.38 M) was added 77% meta-chloroperbenzoic acid (mCPBA) (4.0 eq.) and heated at 60° C. for 20 hours. After cooling to room temperature, Ca(OH)2 (5.3 eq.) was added, and the resulting precipitate was stirred for 30 minutes. The precipitate was filtered and washed with 3:1 CHCl3/methanol. The filtrate was concentrated en vacuo to give a solid, which was stirred in 30% ethyl acetate in hexane and filtered to give the desired N-oxide. The filtrate was concentrated en vacuo, and the residue was purified by a COMBIFLASH® system (ISCO) using 0-100% ethyl acetate in hexane to give more of the desired N-oxide. The two batches were combined and carried onto the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408907B2
Source datasetuspto-grants-2016_08
ORD IDord-eafa71620ecd47729b24578b9a696f22
Source noteuspto-grants-2016_08