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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112369Generated: October 25, 2026

Lithium Bromide → 2-Bromo-6-methylnaphthalene

https://huagongshe.com/reaction/2112369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium BromideHCID 82050—
Reactant6-Bromo-2-naphthyl TrifluoromethanesulfonateHCID 15311216—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-6-methylnaphthaleneHCID 64059247%

Reaction Conditions

Temperature80 °C

Reaction Steps

Under an atmospheric argon gas flow, trifluoromethane sulfonic acid-6-bromo-2-naphthyl ester in an amount of 32 g (90 mmol), dichloro (diphenylphosphinoferrocene)palladium in an amount of 3.6 g (5% by mol), lithium bromide in an amount of 7.8 g (90 mmol) and desiccated tetrahydrofuran in an amount of 100 milliliter were placed into a three neck flask with cooling pipe and having a capacity of 500 milliliter, and then, the resultant solution was cooled down to −20° C. After slowly dripping methylmagnesiumbromide in an amount of 90 milliliter (90 mmol, 1 mol/liter (tetrahydrofuran)) into the flask, the resultant solution was stirred under heating at the temperature of 80° C. for 4 hours. After the reaction terminated, adding dilute hydrochloric acid in an amount of 100 milliliter into the reacted solution, an organic layer was separated and washed with the use of sodium bicarbonate solution and sodium chloride solution, followed by drying with the use of magnesium sulfate. After removing the solvent by distillation by means of a rotary evaporator, the resultant crude product was refined by means of column chromatography (silicagel, hexane/dichloromethane=90/10), and as a result, 9.4 g of aimed compound (white crystal) was obtained (yield: 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524568B2
Source datasetuspto-grants-2009_04
ORD IDord-f80012f87dd846a694b636f3be684a61
Source noteuspto-grants-2009_04