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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258555Generated: November 2, 2026

m-Chloroperbenzoic acid → 6-Bromo-3-fluoro-2-methylpyridine 1-oxide

https://huagongshe.com/reaction/1258555

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant6-Bromo-3-fluoro-2-methylpyridineHCID 2783180—
Reactantsodium thiosulfate NaHCO3HCID 22607107—
SolventDichloromethaneHCID 6344—
Product6-Bromo-3-fluoro-2-methylpyridine 1-oxideHCID 8665311395.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 6-bromo-3-fluoro-2-methylpyridine (2.84 g, 14.94 mmol, 1 eq.) was dissolved in DCM (250 ml) and cooled to 0° C. Then mCPBA (7.34 g, 29.89 mmol, 2 eq.) was added by portions and the reaction was warmed to r.t. and stirred for 48 h. A sat. aqueous solution of NaHCO3/Na2S2O3 (1/1) was added and stirring allowed for 5 min. Then DCM was added and the layers separated. The aqueous layer was extracted with DCM then the organics were combined, dried over MgSO4 and concentrated. 6-bromo-3-fluoro-2-methylpyridine 1-oxide (2.94 g, 89%) was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466176B2
Source datasetuspto-grants-2013_06
ORD IDord-620ae8e3d6f74b5b9a81f51003097f2c
Source noteuspto-grants-2013_06