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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258870Generated: October 26, 2026

Benzyl Bromide → N-benzyl-7-bromo-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/1258870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Bromo-1,2,3,4-tetrahydroquinolineHCID 13865047—
SolventDimethylformamideHCID 6228—
ProductN-benzyl-7-bromo-1,2,3,4-tetrahydroquinolineHCID 4689487171.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 7-bromo-1,2,3,4-tetrahydroquinoline (7.0 g, 33.0 mmol) in DMF (50 mL) was added potassium carbonate (13.6 g, 99.0 mmol), and benzyl bromide (4.33 mL, 36.3 mmol), and the mixture was heated to 60° C. for 12 h, then cooled to room temperature and quenched by the addition of ice-cold water (150 mL). The resulting mixture was extracted with ethyl acetate (3×50 mL), and the organic layers were combined and washed with water (50 mL) and brine (50 mL), then dried over sodium sulfate, concentrated and purified by silica gel column chromatography to furnish 1-benzyl-7-bromo-1,2,3,4-tetrahydro-quinoline (7.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466114B2
Source datasetuspto-grants-2013_06
ORD IDord-06cc487a1729405b8693c02686b23b19
Source noteuspto-grants-2013_06