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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897973Generated: October 31, 2026

Potassium Phosphate, Tribasic → 2,5-diphenylpyridine

https://huagongshe.com/reaction/1897973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantPhenylboronic AcidHCID 66827—
Reactant2,5-DibromopyridineHCID 69353—
Catalyst2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2,5-diphenylpyridineHCID 276285891.8%

Reaction Steps

2,5-dibromopyridine (10 g, 42 mmol), phenylboronic acid (13.4 g, 110 mmol), dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine (S-Phos) (0.7 g, 1.6 mmol), and potassium phosphate (22 g, 105 mmol) were mixed in 200 mL of toluene and 20 mL of water. Nitrogen is bubbled directly into the mixture for 30 minutes. Next, Pd2(dba)3 was added (0.38 g, 0.4 mmol) and the mixture was heated to reflux under nitrogen for 2 h. The mixture was cooled and the organic layer was separated. The organic layers are washed with brine, dried over magnesium sulfate, filtered, and evaporated to a residue. The residue was purified by column chromatography eluting with 10% ethyl acetate/hexanes. 7 g of desired product was obtained after purification. (91.8% yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519384B2
Source datasetuspto-grants-2013_08
ORD IDord-40e2769d76e74b13b3339a09d724b6f7
Source noteuspto-grants-2013_08