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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535244Generated: October 30, 2026

Toluene → HCID 57967304, compound

https://huagongshe.com/reaction/535244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant4-(1-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride)HCID 44119399—
ReactantHCID 57967305HCID 57967305—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 57967304HCID 5796730495.1%

Reaction Steps

In a 50 mL three-neck flask, 0.97 g (2.2 mmol) of 2-[4-(10-bromo-9-anthryl)phenyl]benzoxazole, 0.57 g (2.3 mmol) of 4-(1-naphthyl)phenylboronic acid, 0.46 g (4.3 mmol) of sodium carbonate, 15 mL of toluene, 3 mL of ethanol, and 3 mL of water were placed. The mixture was degassed by being stirred under reduced pressure, and the air in the flask was replaced with nitrogen. To the mixture, 35 mg (0.030 mmol) of tetrakis(triphenylphosphine)palladium(0) was added, and the mixture was stirred under nitrogen stream at 100° C. for 18 hours. After a certain period, water was added to the mixture, and an aqueous layer was extracted with toluene. The obtained extracted solution and the organic layer were combined and washed with a saturated aqueous solution of sodium hydrogen carbonate and saturated saline, and the organic layer was dried with magnesium sulfate. The mixture was gravity filtered, and the obtained filtrate was condensed to give a solid. The solid was purified by silica gel column chromatograghy (toluene:hexane=2:1) and recrystallized with toluene/hexane, giving 1.2 g of the target white powder in a yield of 94%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859108B2
Source datasetuspto-grants-2014_10
ORD IDord-2286aba909da4fcf85f4c8e4c391ee6b
Source noteuspto-grants-2014_10