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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943623Generated: November 2, 2026

Trifluoroacetic acid ethanol → ethyl (2E)-4-aminobut-2-enoate trifluoroacetate

https://huagongshe.com/reaction/1943623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acid ethanolHCID 19378329—
Reactantethyl (2E)-4-(diformylamino)but-2-enoateHCID 58465259—
Productethyl (2E)-4-aminobut-2-enoate trifluoroacetateHCID 72699081—

Reaction Steps

A solution of ethyl (2E)-4-(diformylamino)but-2-enoate (XV) (0.89 mg, 4.8 mmol) in a mixture trifluoroacetic acid-ethanol (absolute) (2:1, 10 mL) was stirred under reflux overnight (the reaction was followed by LC-MS and stopped when complete conversion was achieved). The solvent was evaporated under vacuum to obtain compound ethyl (2E)-4-aminobut-2-enoate trifluoroacetate (IV) as brown oil (undetermined yield), which was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394802B2
Source datasetuspto-grants-2013_03
ORD IDord-c53ed8279bff4145b331eca797379488
Source noteuspto-grants-2013_03