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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864491Generated: November 1, 2026

Trifluoroacetic acid → HCID 131718862, compound

https://huagongshe.com/reaction/864491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantN~2~,N~5~-Bis[hydroxy(phenyl)methylidene]ornithineHCID 184849—
ProductHCID 131718862HCID 131718862—

Reaction Steps

A mixture of the ornithuric acid, as described in Step A, (501.5 g, 1.47 mol) and trifluoroacetic acid (TFAA) (400 ml) was stirred at room temperature for one hour. The resulting solution was evaporated (0.1 Torr) and 1 L of TFAA was added. The solution was stirred for 16 hours and evaporated to dryness (0.01 Torr). Further 1 L of TFAA was added and the solution stirred for 4 hours. Reevaporation of the solution to dryness (0.1 Torr) was followed by addition of further 500 ml of TFAA. The solution was stirred for another 16 hours and evaporated to dryness (0.1 Torr). The oily residue was dissolved in 1.6 L of anhydrous THF and freshly dehydrated oxalic acid (440 g) added to the solution over a period of two hours. Stirring of the mixture was continued for 16 hours, when 7.5 L of ethyl acetate was added. The solution was washed with brine, aqueous sodium bicarbonate (4X), and brine, dried over MgSO4 and evaporated to dryness. Yield of the title compound: 522.8 g (90.5%). Rf=0.33 and 0.27 (eluent: ethyl acetate/petroleum ether 1:1), ketone and its hydrate. m.p.: 113°-115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05563156
Source datasetuspto-grants-1996_10
ORD IDord-b8604c6a6c5c4ff9b85c012bbedb3c5b
Source noteuspto-grants-1996_10