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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072657Generated: October 26, 2026

Oxalyl chloride → Anthraquinone-2-carbonyl Chloride

https://huagongshe.com/reaction/2072657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-Anthraquinonecarboxylic acidHCID 67030—
SolventDichloromethaneHCID 6344—
ProductAnthraquinone-2-carbonyl ChlorideHCID 15025286—

Reaction Steps

The compound of Structure (I-C) was prepared as follows. 2-carboxyanthraquinone was reacted with oxalyl chloride in dichloromethane (catalyzed by dimethylformamide) to yield 2-chlorocarbonylanthraquinone, which was then reacted with 1-hexanol in tetrahydrofuran (in the presence of triethylamine) to yield 2-n-hexoxycarbonylanthraquinone, which was then treated in a manner similar to Preparation A to prepare the Structure (I-C) compound with a yield of 50%. Structure was confirmed by IR and NMR spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04913996
Source datasetuspto-grants-1990_04
ORD IDord-1aade12be2404a799099d9c145ff8cb2
Source noteuspto-grants-1990_04