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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418933Generated: November 1, 2026

2-Methylquinoline → HCID 44239661, compound

https://huagongshe.com/reaction/2418933

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylquinolineHCID 7060—
Reactant3-IodooxetaneHCID 13356686—
ReagentHydrogen PeroxideHCID 784—
ReagentSulfuric AcidHCID 1118—
CatalystCID 516917HCID 516917—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 44239661HCID 4423966132%

Reaction Conditions

Temperature25 °C

Reaction Steps

H2O2 (30% in H2O; 0.31 mL, 3.0 mmol) was added dropwise over 1-2 min to a stirred solution of quinaldine 1b (135 μL, 1.0 mmol), concentrated H2SO4 (107 μL, 2.0 mmol), 3-iodooxetane (368 mg, 2.0 mmol) and iron(II) sulfate heptahydrate (80 mg, 0.3 mmol) in DMSO (10 mL) at room temperature. After 1-2 min a further portion of iron(II) sulfate heptahydrate (80 mg, 0.3 mmol) was added and the mixture was stirred at room temperature for 30 min. Further H2O2(0.31 mL, 3.0 mmol) and iron(II) sulfate heptahydrate (80 mg, 0.3 mmol) was added, and the mixture was stirred for 60 min, then poured into a 0.2 M solution of NaOH (30 mL) and Et2O (50 mL). The aqueous and organic layers were partitioned and the aqueous layer was extracted with Et2O (2 x 25 mL). The combined organic extracts were washed with brine (1 x 30 mL), dried (MgSO4), filtered and the solvent removed under vacuum to leave a crude oil. The oil was purified by preparative thin-layer chromatography using EtOAc / hexanes (3:7) as eluent to give recovered quinaldine 1b (55 mg, 39%), and the desired product 2b (64 mg, 32%) as a solid. An analytical portion of the product 2b was recrystallized from hexanes for data purposes.

Provenance & Evidence

DOI10.1021/jo9010624
Source datasetMinisci dataset from Roche
ORD IDord-fd67d32167634289bf001446bf234950
Source noteMinisci dataset from Roche