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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943009Generated: November 1, 2026

Trifluoroacetic acid → Ethyl 3-amino-2,5-dioxopyrrolidine-3-carboxylate

https://huagongshe.com/reaction/1943009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantethyl 3-[N,N'-bis(tert-butyloxycarbonyl)hydrazino]-2,5-dioxopyrrolidine-3-carboxylateHCID 67342586—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-amino-2,5-dioxopyrrolidine-3-carboxylateHCID 1978542365%

Reaction Steps

To a solution of the compound of Example 4 (970 mg) in dichloromethane (8 ml) was added trifluoroacetic acid (4 ml) and the mixture was stirred at room temperature for 6 hours. The reaction mixture was concentrated and to the resulting residue was added toluene to remove azeotropically the residual trifluoroacetic acid and then the mixture was concentrated again. The residue was dissolved in ethanol (25 ml) and thereto was added an appropriate amount of Raney nickel. This mixture was stirred vigorously at 40° C. under hydrogen (atmospheric pressure) for 24 hours. To the reaction mixture was added water (20 ml) and the mixture was filtered through a Celite pad and then the Celite was washed with ethanol. The mixture of the filtrate combined with the washers was adjusted to pH 7-8 with sodium bicarbonate and then thereto was added pH 7.4 phosphate buffer solution. This mixture was extracted with ethyl acetate and the extract was dried over magnesium sulfate and filtered. The filtrate was concentrated to give an oil which was then purified by a flash column chromatography (chloroform:methanol=20:1→10:1) to give the desired product (292 mg, 65%) as crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389742B2
Source datasetuspto-grants-2013_03
ORD IDord-77dcada3986741a4af0ca141488b5a31
Source noteuspto-grants-2013_03