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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901754Generated: October 29, 2026

Anthraquinone → HCID 22138025, compound

https://huagongshe.com/reaction/901754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnthraquinoneHCID 6780—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(4-Bromophenyl)naphthaleneHCID 5461752—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 22138025HCID 2213802591%

Reaction Conditions

Temperature-20 °C

Reaction Steps

Under an atmosphere of argon, 2-(4-bromophenyl)naphthalene (5.4 g, 19 mmole, 2.8 eq) was dissolved into a mixed solvent composed of anhydrous toluene (25 ml) and anhydrous THF (25 ml) and the resultant solution was cooled at −40° C. in a dry ice/methanol bath. To the cooled solution, a hexane solution of n-butyllithium (1.50 mole/liter, 14 ml, 21 mmole, 1.1 eq) was added and the resultant mixture was stirred at −20° C. for 1 hour. To the resultant solution, anthraquinone (1.4 g, 6.7 mmole) was added and the obtained mixture was stirred at −20° C. for 1 hour and at the room temperature for 3 hours and left standing for one night. To the obtained reaction mixture, a saturated aqueous solution of ammonium chloride (20 ml) was added. The formed solid was separated by filtration and washed with water, methanol and acetone and a white solid (3.7 g, 91%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361796B2
Source datasetuspto-grants-2008_04
ORD IDord-03c10e9b858141208dc2a016fdedb8cb
Source noteuspto-grants-2008_04