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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815674Generated: October 28, 2026

Diphenylamine → HCID 14906272, compound

https://huagongshe.com/reaction/1815674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenylamineHCID 11487—
Reactant3-BromopyridineHCID 12286—
ReactantPotassium HydroxideHCID 14797—
ReactantDi-tert-butylchlorophosphineHCID 139566—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 14906272HCID 14906272—

Reaction Steps

A 30 mL of reactor equipped with magnetic stir bar was charged with 50 mg (0.093 mmol) of (t-Bu)2PCl)2PdCl2, 0.50 g (4.4 mmol) of 3-bromopyridine, 0.50 g (3.16 mmol) of Ph2NH and 0.25 g (4.46 mmol) of KOH in 2 mL of 1,4-dioxane. The reaction mixture was refluxed for 5 hours. The reaction mixture was cooled to room temperature, transferred to a separatory funnel, and diluted with 100 mL of diethyl ether and 20 mL of H2O. The layers were separated, and organic layer was washed with H2O (2×50 mL), brine (30 mL), and dried over MgSO4, filtered, and solvents removed from the filtrate by rotary evaporation. The resulting residue was chromatographed on silicon gel. The eluate was concentrated by rotary evaporation followed by high vacuum to give 3-pyridyldiphenylamine. LC-MS Found: 247.3 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878850B2
Source datasetuspto-grants-2005_04
ORD IDord-3d8904ebd9784e21b39b1f82aa075366
Source noteuspto-grants-2005_04