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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748710Generated: October 31, 2026

2-Bromo-5-methylpyridine → 3-Methyl-2,2'-bipyridine

https://huagongshe.com/reaction/1748710

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-methylpyridineHCID 564216—
Reactant2-(Tributylstannyl)pyridineHCID 607784—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product3-Methyl-2,2'-bipyridineHCID 18245776.2%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2-bromo-5-methylpyridine (5.0 g, 29 mmol), 2-tributylstannylpyridine (10 g, 27 mmol) and Pd(PPh3)4 (2.0 g, 1.7 mmol) in dry toluene (250 mL) was stirred for 48 h at 110° C. The reaction mixture was filtered over Celite and evaporated under reduced pressure. The residue was dissolved in EtOAc and washed with saturated aqueous NaHCO3 solution, and the organic layer was dried over MgSO4 and concentrated under reduced pressure. Flash column chromatography (0.5% MeOH in CH2Cl2) afforded methyl-2,2′-bipyridine (3.5 g, 75%) as a colorless oil. 1H-NMR (500 MHz, CDCl3): 2.47 (s, 3H), 7.35 (dd, 1H), 7.70 (dd, 1H), 7.87 (m, 1H), 8.36 (d, 1H), 8.43 (d, 1H), 8.58 (d, 1H), 8.74 (dd, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150849B2
Source datasetuspto-grants-2015_10
ORD IDord-0b85bad0461c4b31b8c65b9d405da4c7
Source noteuspto-grants-2015_10