Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748951Generated: October 27, 2026

Potassium Phosphate, Tribasic → 2,8-Di(triphenylen-2-yl)dibenzothiophene

https://huagongshe.com/reaction/1748951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2,8-DibromodibenzothiopheneHCID 631120—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant4,4,5,5-Tetramethyl-2-(triphenylen-2-yl)-1,3,2-dioxaborolaneHCID 58769449—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2,8-Di(triphenylen-2-yl)dibenzothiopheneHCID 5948923894%

Reaction Steps

2.25 g (6.3 mmol) of 4,4,5,5-tetramethyl-2-(triphenylen-2-yl)-1,3,2-dioxaborolane, 0.92 g (2.7 mmol) of 2,8-dibromodibenzothiophene, 0.12 g (0.14 mmol) of Pd2(dba)3, 0.22 g (0.53 mmol) of 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl, 3.4 g (16.0 mmol) of K3PO4, 100 mL of toluene and 10 mL of water were charged in a 250 mL round bottom flask. The reaction mixture was purged with nitrogen for 20 min and then heated up to reflux for overnight with stirring. The reaction mixture was cooled and filtered. The white solid was washed with methanol 3 times (3×100 mL) and methylene chloride (2×100 mL). 1.6 g of (94% yield) solid was obtained as the product which was further purified by recrystallization with toluene and sublimation. The product was confirmed by solid probe MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09153786B2
Source datasetuspto-grants-2015_10
ORD IDord-aaaf0e4c09c74dda8137c5aaae74322e
Source noteuspto-grants-2015_10