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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201020Generated: October 29, 2026

Toluene → HCID 66687323, compound

https://huagongshe.com/reaction/2201020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactanto-IodonitrobenzeneHCID 69115—
Reactant(6-Phenylpyridin-3-yl)boronic acidHCID 2762710—
Catalyst2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
SolventWaterHCID 962—
ProductHCID 66687323HCID 6668732365.7%

Reaction Steps

2-Iodo-1-nitrobenzene (6.88 g, 27.64 mmol), 6-phenyl-3-pyridinylboronic acid (5.5 g, 27.64 mmol), potassium phosphate (17.6 g, 82.91 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (0.451 g, 0.522 mmol) and Pd2(bda)3 (0.119 g, 0.55 mmol) were to toluene (150 mL) and water (12 mL). Nitrogen was bubbled through the solution for 30 minutes and then the solution was refluxed for overnight in an atmosphere of nitrogen. The reaction was then allowed to cool to room temperature and the organic phase was separated from the aqueous phase. The aqueous phase was extracted with ethylacetate and the organic fractions were combined and dried over sodium sulfate and the solvent removed under vacuum. The product was chromatographed using silica gel with ethylacetate and hexanes as the eluent. The solvent was removed to give 5.02 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359549B2
Source datasetuspto-grants-2016_06
ORD IDord-9378ef9515b548f4afc4380f4a687405
Source noteuspto-grants-2016_06