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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797387Generated: October 26, 2026

Sodium Carbonate → [1,1':2',1''-Terphenyl]-2-amine

https://huagongshe.com/reaction/1797387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant2,6-DibromoanilineHCID 69098—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product[1,1':2',1''-Terphenyl]-2-amineHCID 1259549790%

Reaction Steps

2,6-Dibromoaniline (6.02 g, 24 mmol) and Pd(PPh3)4 (3.88 g, 3.00 mmol) were dissolved in toluene (240 ml). Phenyl boronic acid (8.80 g, 72 mmol) in EtOH (50 ml) was added. Na2CO3 (13 g, 144 mmol) in H2O (70 ml) was added. The reaction mixture was reflux for 24 hrs. The organic layer was thin separated and the amine precipitated as hydrochloride salt by addition of 20 ml of HCl. The precipitate was isolated. The salt was suspended in ether, and 2 M Na2CO3 was added. The organic layer was dried over Na2SO4 and the solvent was evaporated. The yield was 90%. 1H NMR (CDCl3): δ 7.44 (t, 4H, Harom), 7.39 (t, 4H, Harom), 7.29 (d, 2H, Harom), 7.07 (d, 2H, Harom), 6.82 (t, 1H, Harom), 3.77 (s, 2H, NH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034157B2
Source datasetuspto-grants-2006_04
ORD IDord-1fcad542f0344c99b2dab2bb67a279b4
Source noteuspto-grants-2006_04