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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852558Generated: November 1, 2026

N-phenyl-2-naphthylamine → HCID 58078267, compound

https://huagongshe.com/reaction/1852558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-phenyl-2-naphthylamineHCID 8679—
ReactantPyrene, 1,6-Dibromo-HCID 176470—
ReactantSodium t-butoxideHCID 23676156—
CatalystPalladium (II) acetateHCID 4144353—
SolventTolueneHCID 1140—
ProductHCID 58078267HCID 5807826737%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 18 g (50 mmol) of 1,6-dibromopyrene, 11 g (50 mmol) of N-phenylnaphthalen-2-amine, 0.16 g (0.7 mmol) of Pd(OAC)2, 0.5 g (1.4 mmole) of tri-tert-butylphosine, 6 g (75 mmol) sodium tert-butoxide was stirred in 200 ml dry toluene, the reaction mixture was then heat to 100° C. for about overnight under nitrogen. The solution was filtered. The toluene solution was removed under reduced pressure from the filtrate. The residue was extracted three times with dichloromethane and water, dried with MgSO4 and filtered, and the dichloromethane was removed under reduced pressure. The product was purified by column chromatography to get 9.2 g of product (yield 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962160B2
Source datasetuspto-grants-2015_02
ORD IDord-3236bfe73071403eb06e9252f592abf6
Source noteuspto-grants-2015_02