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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424244Generated: October 26, 2026

Hydrogen Peroxide → 3-METHYLQUINOLINE N-OXIDE

https://huagongshe.com/reaction/1424244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium IodideHCID 5238—
Reactant3-MethylquinolineHCID 11926—
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfiteHCID 24437—
SolventAcetic AcidHCID 176—
Product3-METHYLQUINOLINE N-OXIDEHCID 7021466—

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Methylquinoline (30.0 mL, 224 mmol) was dissolved in acetic acid (85 mL), and 30% aqueous hydrogen peroxide (30.4 mL) was added. The reaction was stirred at 80° C. for 16 h before cooling in an ice bath. 10% aq Na2SO3 (199 mL, 0.5 equiv) was added followed by sodium iodide (2.358 g, 0.05 equiv). This mixture was stirred for 5 min. A peroxide test strip indicated no peroxide remaining. 5N aq NaOH was then added, keeping the internal temperature below 24° C. A dark color formed, indicating that the solution was basic (tested as pH 10). The solution was extracted with four portions of dichloromethane. The combined organics were dried over MgSO4 and filtered, and the filtrate was concentrated under reduced pressure. Purification by silica gel flash chromatography (methanol/ethyl acetate) gave 3-methylquinoline 1-oxide (Intermediate 3, 32.09 g) as a yellow solid. 1H NMR (400 MHz, CDCl3) δ 8.69 (d, J=8.8 Hz, 1H), 8.42 (s, 1H), 7.77 (d, J=8.2 Hz, 1H), 7.68 (td, J=7.8, 1.1 Hz, 1H), 7.56-7.63 (m, 1H), 7.52 (s, 1H), 2.45 (s, 3H); MS (M+1): 160.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927577B2
Source datasetuspto-grants-2015_01
ORD IDord-67022b90266642e0bb29a047f1c02af0
Source noteuspto-grants-2015_01