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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201119Generated: October 28, 2026

Benzyl 1-amino-4,4,4-trifluoro-1-oxobutan-2-ylcarbamate → 2-Amino-4,4,4-trifluorobutanamide

https://huagongshe.com/reaction/2201119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 1-amino-4,4,4-trifluoro-1-oxobutan-2-ylcarbamateHCID 67515558—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-Amino-4,4,4-trifluorobutanamideHCID 4471737293.5%

Reaction Steps

A solution of benzyl 1-amino-4,4,4-trifluoro-1-oxobutan-2-ylcarbamate (175 mg, 0.603 mmol) and Pd—C (10%, 55 mg) in MeOH (5 mL) was hydrogenated under balloon hydrogen for 2 h. The mixture was filtered through celite. The filtrate was concentrated in vacuo to give 2-amino-4,4,4-trifluorobutanamide (88 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359375B2
Source datasetuspto-grants-2016_06
ORD IDord-d9a282c4ce7e4173a232a8f9646d384f
Source noteuspto-grants-2016_06