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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216338Generated: October 25, 2026

Benzyl Bromide → 2-Benzyl-6-methoxypyridine

https://huagongshe.com/reaction/2216338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTetrahydrofuranHCID 8028—
Reactant2-Bromo-6-methoxypyridineHCID 256810—
ReactantMagnesiumHCID 5462224—
CatalystDiphenylphosphane;diphenyl(propan-2-yl)phosphane;nickel;chlorideHCID 21654969—
SolventDiethyl EtherHCID 3283—
Product2-Benzyl-6-methoxypyridineHCID 21942274—

Reaction Steps

While stirring a mixture of 150 g of 2-bromo-6-methoxypyridine, 4.3 g of 1,3-bis(diphenylphosphino)propanenickel (II) chloride and 500 ml of tetrahydrofuran in an ice bath, Grignard reagent prepared from 123 ml of benzyl bromide, 30 g of magnesium and 400 ml of diethyl ether was added dropwise slowly. After stirring overnight as it was, the mixture was extracted with an aqueous ammonium chloride solution and hexane. The organic layer was washed with water and then with brine, dried over anhydrous magnesium sulfate, and the solvent was removed. The residue was purified by silica gel column chromatography with (1% ethyl acetate/hexane and 1.5% ethyl acetate/hexane), to give 150 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112593B2
Source datasetuspto-grants-2006_09
ORD IDord-cb11222e764849c083897a8941c8501e
Source noteuspto-grants-2006_09