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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755514Generated: October 26, 2026

Phenyl-1-naphthylamine → N-(4'-bromo-[1,1'-biphenyl]-4-yl)-N-phenylnaphthalen-1-amine

https://huagongshe.com/reaction/1755514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl-1-naphthylamineHCID 7013—
Reactant4,4'-DibromobiphenylHCID 7110—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTolueneHCID 1140—
ProductN-(4'-bromo-[1,1'-biphenyl]-4-yl)-N-phenylnaphthalen-1-amineHCID 1675531262%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of N-phenylnaphthalen-1-amine (4.41 g, 20 mmol), 4,4′-dibromo-1,1′-biphenyl (15 g, 48 mmol), sodium tert-butoxide (NaOBut) (4.8 g, 50 mmol) and Pd(dppf)Cl2 (0.44 g, 0.6 mmol) in anhydrous toluene (100 mL) was degassed and heated at 80° C. for about 10 hours. After cooling to RT, the mixture was poured into dichloromethane (400 mL) and stirred for about 30 min., then washed with brine (100 mL). The organic solution was collected and dried over Na2SO4, loaded on silica gel, and purified by flash column (hexanes to hexanes/ethyl acetate 90:1) to give a solid which was washed with methanol and dried under air to give a white solid Compound 4 (5.58 g, in 62% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09172051B2
Source datasetuspto-grants-2015_10
ORD IDord-bb1c2452679d4f3d8feb4e1f7f9f8309
Source noteuspto-grants-2015_10