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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713555Generated: November 3, 2026

Toluene → HCID 71007966, compound

https://huagongshe.com/reaction/713555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTrimethylboroxineHCID 574072—
ReactantPotassium phosphate, tribasic, monohydrateHCID 22031701—
ReactantHCID 71007915HCID 71007915—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Catalyst2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
SolventWaterHCID 962—
ProductHCID 71007966HCID 71007966—

Reaction Steps

5-Bromo-2-(dibenzo[b,d]furan-4-yl)-4-methylpyridine (28.7 g, 85 mmol), dicyclohexyl(2′,6′-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine (1.394 g, 3.39 mmol) and potassium phosphate monohydrate (58.6 g, 255 mmol) were added to toluene (500 mL) and water (50 mL) and degassed for 20 min. Trimethylboroxine (14.83 mL, 106 mmol) and Pd2(dba)3 (0.777 g, 0.849 mmol) were added and the reaction mixture heated to reflux overnight. After cooling, the organic layer was separated and the aqueous layer extracted 3×50 mL with EtOAc, dried over sodium sulfate and evaporated. The crude product was chromatographed on silica gel with 8/2 (v/v) dichloromethane/EtOAc in hexane to give 19.2 g of an off-white solid, which was recrystallized from heaxane to give 16.8 g (83%) of the product as white needles. The product was confirmed by NMR and HPLC (99.97% pure).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09184397B2
Source datasetuspto-grants-2015_11
ORD IDord-1a2a675ba1694204a4679220da029d13
Source noteuspto-grants-2015_11