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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874919Generated: October 30, 2026

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

https://huagongshe.com/reaction/874919

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 numberUS08981092B2
Source datasetuspto-grants-2015_03
ORD IDord-48f87ce256fd4089aa33cc6700a88f3b
Source noteuspto-grants-2015_03