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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901766Generated: October 25, 2026

Sodium Carbonate → 9-(4-(2,2-Diphenylvinyl)phenyl)-10-(4-(2-phenylvinyl)phenyl)anthracene

https://huagongshe.com/reaction/901766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(4-(2,2-Diphenylvinyl)phenyl)boronic acidHCID 11392411—
Reactant9-Bromo-10-(4-(2-phenylvinyl)phenyl)anthraceneHCID 73866852—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTolueneHCID 1140—
Product9-(4-(2,2-Diphenylvinyl)phenyl)-10-(4-(2-phenylvinyl)phenyl)anthraceneHCID 7386685388%

Reaction Steps

Under an atmosphere of argon, 9-bromo-10-(4-(2-phenylvinyl)-phenyl)anthracene (3.1 g, 7.1 mmole), 4-(2,2-diphenylvinyl)phenylboronic acid (2.4 g, 8.0 mmole, 1.1 eq) and tetrakis(triphenylphosphine)-palladium(0) (0.16 g, 0.14 mmole, 2% Pd) were suspended into toluene (25 ml). To the obtained suspension, a 2 M aqueous solution of sodium carbonate (2.5 g, 24 mmole, 3 eq/12 ml) was added and the resultant mixture was heated under refluxing for 10 hours. The reaction mixture was filtered and washed with water and methanol and a yellow solid was obtained. The obtained solid was suspended in boiling toluene (50 ml), cooled while being left standing, filtered and washed with toluene and a light yellow solid (3.8 g, 88%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361796B2
Source datasetuspto-grants-2008_04
ORD IDord-d3ed411092ed473a9b0023ebd237e5f9
Source noteuspto-grants-2008_04