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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944075Generated: October 26, 2026

Sodium Iodide → 6-Bromo-1-(4-methoxy-benzyl)-1,2,3,4-tetrahydro-quinoline

https://huagongshe.com/reaction/1944075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
Reactant6-Bromo-1,2,3,4-tetrahydroquinolineHCID 4715029—
SolventDimethylformamideHCID 6228—
Product6-Bromo-1-(4-methoxy-benzyl)-1,2,3,4-tetrahydro-quinolineHCID 5834085362.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 6-bromo-1,2,3,4-tetrahydro-quinoline (3.00 g, 12.1 mmol) in dimethylformamide (25 ml) was added potassium carbonate (3.3 g, 24.1 mmol), sodium iodide (0.905 g, 6.0 mmol) and 4-methoxybenzyl chloride (2.5 ml, 18.1 mmol) and heated at 50° C. After 18 h, reaction mixture was cooled to room temperature and quenched by the addition of water and extracted with ethyl acetate (2×20 ml). The organic layer was washed with water (2×20 mL), brine (20 mL), dried over sodium sulfate, concentrated and purified by the silica gel column chromatography to furnish 6-bromo-1-(4-methoxy-benzyl)-1,2,3,4-tetrahydro-quinoline (2.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394772B2
Source datasetuspto-grants-2013_03
ORD IDord-ebde4235801b441dadcca826684b0cb0
Source noteuspto-grants-2013_03