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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128073Generated: October 25, 2026

Formic Acid → HCID 23471363, compound

https://huagongshe.com/reaction/128073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantTetrahydrofuranHCID 8028—
Reactant2-HydroxyanthraquinoneHCID 11796—
ProductHCID 23471363HCID 23471363—

Reaction Steps

In the same system as described for the 2,6-dihydroxy analog, a solution of 0.01 mole of the silated 2-hydroxy-anthraquinone in tetrahydrofuran is treated slowly with a solution of 0.01 mole of the same lithio anion. The reaction is allowed to proceed for two hours at room temperature. This solution of the enamine is hydrolyzed at room temperature by addition of 20 ml. of 90% formic acid solution. The reaction mixture is filtered, washed with water, dried and recrystallized from toluene giving 2-hydroxy-9,10-anthracene dicarboxaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04258181
Source datasetuspto-grants-1981_03
ORD IDord-a708f0a226a242abb0bbb7db995b1bfb
Source noteuspto-grants-1981_03