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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755711Generated: November 2, 2026

Thionyl Chloride → Acridine-9-carbonyl chloride hydrochloride

https://huagongshe.com/reaction/1755711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantAcridine-9-carboxylic acidHCID 94721—
ProductAcridine-9-carbonyl chloride hydrochlorideHCID 1239593096%

Reaction Steps

Acridine-9-carboxylic acid (0.42 g, 1.87 mmol) was suspended in thionyl chloride (10 ml) and the suspension was refluxed under heating for 2 h. Excess thionyl chloride was distilled off the reaction mixture under reduced pressure to give 9-chlorocarbonylacridine hydrochloride (0.5 g, 96%). Then, the resulting 9-chlorocarbonylacridine hydrochloride (0.5 g) and 2-methylphenol (0.2 g, 1.9 mmol) were suspended in dichloromethane (15 ml) and triethylamine (1.0 ml) and a catalytic amount of dimethylaminopyridine were added to the suspension with stirring. The reaction mixture was stirred at room temperature for 15 h and thereafter washed with 1 N HCl, water, a 5% aqueous solution of sodium hydrogencarbonate and a saturated aqueous solution of sodium chloride in the order written. The organic layer was separated and dried over anhydrous sodium sulfate, followed by evaporation of the solvent under reduced pressure. The residue was purified by silica gel column chromatography using a dichloromethane-hexane mixture as eluant, giving the desired compound, 2'-methylphenyl acridine-9-carboxylate, in an amount of 0.33 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438139
Source datasetuspto-grants-1995_08
ORD IDord-7e77992a60224db289db825dc97a9212
Source noteuspto-grants-1995_08