Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039430Generated: October 29, 2026

1,3-Dibromobenzene → 4-(3'-Bromobiphenyl-3-yl)dibenzothiophene

https://huagongshe.com/reaction/2039430

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromobenzeneHCID 7927—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(3-(Dibenzo[b,d]thiophen-4-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 59575355—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-(3'-Bromobiphenyl-3-yl)dibenzothiopheneHCID 6697446279.3%

Reaction Steps

2-(3-(dibenzo[b,d]thiophen-4-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (8.80 g, 22.78 mmol) and 1,3-dibromobenzene (21.49 g, 91 mmol) were dissolved in toluene (300 mL), and potassium carbonate (9.44 g, 68.3 mmol) in 50 mL of water and the Pd(PPh3)4 catalyst (0.263 g, 0.228 mmol) were then added. The reaction mixture was degassed and refluxed under N2 overnight. The organic layer was then separated, evaporated and subjected to column chromatography on silica gel, eluted with hexane/DCM 9:1 v/v mixture, providing 4-(3′-bromo-[1,1′-biphenyl]-3-yl)dibenzo[b,d]thiophene (7.5 g, 18.06 mmol, 79% yield) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580399B2
Source datasetuspto-grants-2013_11
ORD IDord-9b3d76d80e424dd29b9bb938ddf6ac45
Source noteuspto-grants-2013_11