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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274136Generated: October 29, 2026

Hydrochloric Acid → HCID 67607343, compound

https://huagongshe.com/reaction/2274136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
Reactant6-Bromo-2-naphthalenolHCID 27144—
ReactantFluoranthen-3-ylboronic acidHCID 23088535—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 67607343HCID 6760734389.1%

Reaction Steps

Under the atmosphere of argon, 2.7 g of fluoranthene-3-boronic acid, 2.0 g of 6-bromo-2-naphthol, 0.31 g of tetrakis(triphenylphosphine)palladium (0), 27 mL of 1,2-dimethoxyethane and 13.5 mL of an aqueous 2M sodium carbonate solution were placed in a flask, and the resulting mixture was stirred under reflux while heating for 4 hours. After cooling to room temperature, 2M hydrochloric acid was added to the reaction solution to allow it to be acidic, and the reaction solution was extracted with dichloromethane. An aqueous phase was removed and an organic phase was washed with saturated saline, and dried with anhydrous sodium sulfate. After filtration, the solvent was distilled off under reduced pressure, residues were dispersed and washed with dichloromethane, whereby 2.75 g (yield 89%) of 6-(fluoranthen-3-yl)-2-naphthol as an intended product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126943B2
Source datasetuspto-grants-2015_09
ORD IDord-15ca47a75e064c1b9549e6405a7603d5
Source noteuspto-grants-2015_09