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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848956Generated: November 2, 2026

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

https://huagongshe.com/reaction/1848956

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 numberUS08952363B2
Source datasetuspto-grants-2015_02
ORD IDord-661b6b06ede444cfb801494f7e2323f7
Source noteuspto-grants-2015_02