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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539492Generated: October 23, 2026

Toluene → HCID 70654352, compound

https://huagongshe.com/en/reaction/539492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734652—
Reactant2-Bromo-5-methoxybenzonitrileHCID 21784096—
ReactantPotassium phosphate, tribasic, monohydrateHCID 22031701—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
ProductHCID 70654352HCID 7065435268%

Reaction Steps

2-Bromo-5-methoxybenzonitrile (1.32 g, 6.23 mmol), 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (1.36 g, 6.23 mmol), bis(triphenylphosphine)palladiumdichloride (0.437 g, 0.623 mmol) and potassium phosphate monohydrate (4.30 g, 18.68 mmol) were added to toluene (30 mL) and water (3 mL). The reaction mixture was degassed with bubbled nitrogen gas for 30 minutes before being refluxed under nitrogen for 15 h. After cooling, the reaction mixture was filtered through Celite® and the organic layer was extracted with ethyl acetate. After removal of the solvents, the crude material was triturated with 40 mL of DCM followed by 50 mL of hexanes to give 8-methoxyphenanthridin-6-amine (0.95 g, 68%) as a light yellow solid. The product was confirmed by GC/MS and NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871361B2
Source datasetuspto-grants-2014_10
ORD IDord-64e2c143a486468fb1914509aa94df46
Source noteuspto-grants-2014_10