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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910346Generated: November 1, 2026

1,2-Dimethoxyethane → 2-(4-Bromophenyl)-5-methylpyridine

https://huagongshe.com/reaction/1910346

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Bromophenyl)boronic acidHCID 79599—
Reactant2-Bromo-5-methylpyridineHCID 564216—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-(4-Bromophenyl)-5-methylpyridineHCID 1195457791.9%

Reaction Steps

To a 500 mL round bottom flask, 4-bromophenylboronic acid (25.0 g, 0.125), 2-bromo-5-methylpyridine (20.0 g, 0.114 mol), palladium(0)tetrakistriphenylphosphine (4.0 g, 0.0035 mol), potassium carbonate (47.0 g, 0.34 mol.), 1,2-dimethoxyethane (120 mL) and water (120 mL.) were added. The mixture was heated to reflux under nitrogen atmosphere for 18 hours. After the reaction was cooled down, 100 mL of water and 150 mL of ethyl acetate were added. The mixture was separated in a separatory funnel. The organic phases were collected, combined and evaporated. The mixture was distilled using a kugelrohred (spelling?) to obtain 2-(4-bromophenyl)-5-methylpyridine (26.0 g) as a white solid that was further purified by recrystallization in hexanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08603645B2
Source datasetuspto-grants-2013_12
ORD IDord-8ba0a61fb6ef42fd991796d4b13720a3
Source noteuspto-grants-2013_12