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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713564Generated: October 26, 2026

Toluene → 5-Methyl-2-phenylpyridine

https://huagongshe.com/reaction/713564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-Bromo-5-methylpyridineHCID 564216—
ReactantPotassium phosphate, tribasic, monohydrateHCID 22031701—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Catalyst2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
SolventWaterHCID 962—
Product5-Methyl-2-phenylpyridineHCID 4746788.3%

Reaction Steps

2-Bromo-5-methylpyridine (30 g, 174 mmol), phenylboronic acid (25.5 g, 209 mmol), dicyclohexyl(2′,6′-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine (2.86 g, 6.98 mmol) and potassium phosphate tribasic monohydrate (120 g, 523 mmol) were added to toluene (600 mL) and water (60 mL). The reaction mixture was degassed with nitrogen for 20 min. Pd2(dba)3 (3.19 g, 3.49 mmol) was added and the reaction mixture was refluxed for 18 h. After cooling, the organic layer was separated and the aqueous layer extracted with 3×50 mL dichloromethane, dried over sodium sulfate and evaporated. The crude product was chromatographed on silica gel with 75/25 (v/v) hexane/EtOAc and then distilled on a Kugelrohr apparatus (150° C., 100 mbar) to give 26 g (88%) of 5-methyl-2-phenylpyridine as a white solid. The product was confirmed by NMR and GC/MS. HPLC purity: 99.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09184397B2
Source datasetuspto-grants-2015_11
ORD IDord-3696a75dda6f4de794b2f810fe82a3af
Source noteuspto-grants-2015_11