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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741811Generated: October 25, 2026

Aniline → Itaconic acid

https://huagongshe.com/reaction/1741811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantMethylsuccinic acidHCID 10349—
ReactantDicyclohexylcarbodiimideHCID 10868—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductItaconic acidHCID 811—

Reaction Steps

The enantiomer excess (hereinafter referred to as "e.e.") of the resulting methylsuccinic acid was determined as follows. A part (1.32 mg, 0.1 mmole) of the crude product was dissolved in 2 ml of THF and 2 ml of acetonitrile, and 45.4 mg (0.22 mmole) of N,N'-dicyclohexylcarbodiimide, 2.4 mg (0.02 mmole) of 4-dimethylaminopyridine, and 0.01 ml (0.11 mmole) of aniline were added to the solution, followed by stirring at room temperature overnight. The solvent was removed from the reaction mixture by distillation under reduced pressure. The residue was dissolved in chloroform, washed three times with a 5M hydrochloric acid aqueous solution and then once with a saturated sodium hydrogencarbonate aqueous solution in a successive manner, and dried over magnesium sulfate. The solvent was removed, and the crude dianilide was purified by silica gel column chromatography using diethyl ether as an eluent. The purified dianilide was subjected to high performance liquid chromatography (HPLC) using a chromatograph equipped with CHIRALCEL-OD® (manufactured by Daicel Chemical Industries, Ltd.) (eluent: isopropyl alcohol/hexane=10/90 by volume; detection: UV 254 nm; flow rate: 1 ml/min) to determine the e.e.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05334758
Source datasetuspto-grants-1994_08
ORD IDord-c816918279b4438eb3824c7bb3b52382
Source noteuspto-grants-1994_08