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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045745Generated: November 1, 2026

2-Bromoanthraquinone → HCID 69032464, compound

https://huagongshe.com/reaction/2045745

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoanthraquinoneHCID 221013—
ReactantHCID 178506676HCID 178506676—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69032464HCID 69032464—

Reaction Steps

In a 300 mL three-neck flask was put 4.90 g (17.0 mmol) of 2-bromo-9,10-anthraquinone, and the atmosphere in the flask was replaced with nitrogen. To the flask was added 100 mL of tetrahydrofuran (THF), and 17.8 mL (37.3 mmol) of phenyllithium was dropped into this solution. After the completion of the dropping, this solution was stirred at room temperature for 15 hours. Then, this solution was washed with water, and the aqueous layer was extracted with ethyl acetate. The extract solution and the organic layer were combined and dried with magnesium sulfate. Then, this mixture was gravity filtered. The obtained filtrate was concentrated to give 2-bromo-9,10-dihydroanthracene-9,10-diol, which was the object of the synthesis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592053B2
Source datasetuspto-grants-2013_11
ORD IDord-6b5a96933e5c4c90ae1335344a9ba63f
Source noteuspto-grants-2013_11