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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888683Generated: October 25, 2026

2-Bromoanthraquinone → 2-Bromo-9,10-diphenyl-9,10-dihydroanthracene-9,10-diol

https://huagongshe.com/reaction/888683

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoanthraquinoneHCID 221013—
ReactantHCID 178506676HCID 178506676—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-9,10-diphenyl-9,10-dihydroanthracene-9,10-diolHCID 23160218—

Reaction Steps

4.9 g (17 mmol) of 2-bromo-9,10-anthraquinone was put in a 300 mL three-neck flask, the atmosphere in the flask was substituted by nitrogen, and 100 mL of tetrahydrofuran (THF) was added thereto and dissolved well. Then, 18 mL (37 mmol) of phenyllithium was dropped into this solution and stirred at room temperature for approximately 12 hours. After reaction, the solution was washed with water, and an aqueous layer was extracted with ethyl acetate. The extracted solution and an organic layer were dried with magnesium sulfate. After drying, the mixture was subjected to suction filtration, and the filtrate was concentrated, so that 2-bromo-9,10-diphenyl-9,10-dihydroanthracene-9,10-diol (about 7.6 g), which was the object of the synthesis, was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08251765B2
Source datasetuspto-grants-2012_08
ORD IDord-b365f05febbb4a008e8cd26da89c3571
Source noteuspto-grants-2012_08