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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505383Generated: October 26, 2026

Hydrochloric Acid → 2-Chloro-3-methyl-1-oxo-1lambda~5~-pyridine

https://huagongshe.com/reaction/505383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantUreaHCID 1176—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium DithioniteHCID 24489—
ReactantCarbamide PeroxideHCID 31294—
Reactant2-Chloro-3-methylpyridineHCID 87603—
SolventDichloromethaneHCID 6344—
Product2-Chloro-3-methyl-1-oxo-1lambda~5~-pyridineHCID 1343162263%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a mixture of 2-chloro-3-methylpyridine (12.8 g, 100 mmol), urea hydrogen peroxide addition compound ((NH2)2CO.H2O2, 19.8 g, 210 mmol) and dichloromethane (130 ml) was added dropwise anhydrous trifluoroacetic acid (28.2 ml, 200 mmol) at 0° C. under nitrogen flow, and the reaction mixture was stirred at 0° C. for 1 hour. Then, after stirring for 30 minutes and elevating the reaction temperature to room temperature, an aqueous solution (200 ml) of sodium hydrosulfite (20 g) was added, and the reaction mixture was stirred for 15 minutes. 2N hydrochloric acid (50 ml) was added and the mixture was extracted with dichloromethane (120 ml), and after washed with sodium bicarbonate solution, the mixture was dried over magnesium sulfate and the solvent was evaporated, thereby yielding the title compound (9.00 g, 62.7 mmol, 63%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781452B2
Source datasetuspto-grants-2010_08
ORD IDord-ed9b942820084dbeb4e4a32f7027b488
Source noteuspto-grants-2010_08