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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178738Generated: October 31, 2026

Toluene → 3-chloro-6-(2-triphenyleneyl)-[1]Benzothieno[2,3-c]pyridine

https://huagongshe.com/reaction/2178738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTriphenylen-2-ylboronic acidHCID 59805119—
Reactant3-Chloro-6-bromo-[1]benzothieno[2,3-c]pyridineHCID 86643577—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Catalyst2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
SolventWaterHCID 962—
Product3-chloro-6-(2-triphenyleneyl)-[1]Benzothieno[2,3-c]pyridineHCID 8664357670%

Reaction Steps

The mixture of 3-chloro-6-bromo-[1]benzothieno[2,3-c]pyridine (1.7 g, 5.8 mmol), triphenylen-2-ylboronic acid (1.6 g, 5.8 mmol), potassium phosphate tribasic (3.7 g, 17 mmol), 200 mL toluene and 10 mL water was prepared and bubbled with nitrogen for twenty minutes. Then the tris(dibenzylideneacetone)dipalladium (53 mg, 0.060 mmol) and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (96 mg, 0.23 mmol) were added. The mixture was bubbled with nitrogen for another twenty minutes. After refluxed overnight under nitrogen, then reaction mixture was cooled to room temperature and filtered through a silica plug and washed with dichloromethane. The first several portions were discarded since they only contained impurities. The combined filtrate was concentrated to give crude product, which was recrystallized from hot dichloromethane and hexanes to give 1.8 g 3-chloro-6-(2-triphenyleneyl)-[1]Benzothieno[2,3-c]pyridine as yellow solid (4.0 mmol, 70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067947B2
Source datasetuspto-grants-2015_06
ORD IDord-00b28203e81b4c78bc2f9352b24d6721
Source noteuspto-grants-2015_06