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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402206Generated: November 2, 2026

2-Aminobiphenyl → HCID 13275278, compound

https://huagongshe.com/reaction/402206

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobiphenylHCID 7015—
Reactant2-BromobiphenylHCID 16329—
Reactantsodium 2-methylpropan-2-olateHCID 178418730—
CatalystTris(1,1-dimethylethyl)phosphineHCID 83681—
SolventTolueneHCID 1140—
ProductHCID 13275278HCID 1327527871%

Reaction Conditions

Temperature110 °C

Reaction Steps

Trisdibenzylideneacetonedipalladium (0.276 g, 0.3 mmol) and tri-tert-butylphosphine (0.121 g, 0.6 mmol) were put into a flask, and then dissolved in 40 mL of toluene. Subsequently, 2-biphenylamine (2.53 g, 15 mmol), 2-bromobiphenyl (3.50 g, 15 mmol) and tert-butoxy sodium (2.16 g, 22.5 mmol) were added into the flask, and then refluxed at a temperature of 110° C. for 12 hours. After the flask including the reactant mixture was cooled to room temperature, the reactant mixture was washed using an ammonium chloride aqueous solution (150 mL) to separate an organic layer. The separated organic layer was washed with distilled water three times, and was then dried with magnesium sulfate. Thereafter, residues from which volatile components were removed at reduced pressure were purified using a silica gel chromatography tube in a mixed solvent of hexane and ethylacetate (1:10), and were then recrystallized in normal hexane to produce 3.42 g of dibiphenyl-2-yl amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742043B2
Source datasetuspto-grants-2014_06
ORD IDord-dc633752e1664d5982725f862cd2ef57
Source noteuspto-grants-2014_06