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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7135Generated: October 26, 2026

3-Bromoquinoline → 3-Methoxyquinoline

https://huagongshe.com/reaction/7135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromoquinolineHCID 21413—
ReactantSodium MethoxideHCID 10942334—
SolventDimethylformamideHCID 6228—
Product3-MethoxyquinolineHCID 5758076.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 3-bromoquinoline (22.54 g, 108 mmol) in anhydrous DMF (110 mL) was treated with sodium methoxide (11.70 g, 217 mmol) and stirred at 80° C. for 16 hours. The reaction mixture was then concentrated and the residue taken up in ethyl acetate (300 mL) and water (60 mL). The organic phase was separated, washed with brine (2×60 mL), dried (MgSO4), filtered, concentrated and purified by column chromatography on silica gel (ethyl acetate/hexane; 1:3) to give 3-methoxyquinoline (1.06 g, 6%). 1H NMR (CDCl3) δ 3.95 (s, 3H), 7.38 (d, 1H, J=1.5 Hz), 7.54 (m, 2H), 7.72 (d, 1H, J=7.5 Hz), 8.04 (d, 1H, J=7.5 Hz), 8.67 (d, 1H, J=1.5 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084155B2
Source datasetuspto-grants-2006_08
ORD IDord-5203239c158e446e9e84abab6abb16bf
Source noteuspto-grants-2006_08