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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880935Generated: October 30, 2026

Trifluoroacetic acid → Ethyl 2-((cyclopentylamino)methyl)-2-fluorobutanoate

https://huagongshe.com/reaction/1880935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl 2-((benzyl(cyclopentyl)amino)methyl)-2-fluorobutanoateHCID 57955532—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
ProductEthyl 2-((cyclopentylamino)methyl)-2-fluorobutanoateHCID 5795559088%

Reaction Steps

A solution of ethyl 2-((benzyl(cyclopentyl)amino)methyl)-2-fluorobutanoate (2.2 g, 6.8 mmol) in ethanol (20 mL) was hydrogenated with Pd(OH)2 (20%, 240 mg, 0.34 mmol) in presence of TFA (6.8 mmol) at atmospheric pressure for 20 h. The reaction mixture was filtered through celite. The filtrate was concentrated and diluted to EtOAc/H2O, aqueous layer was basified to pH=11-12 by 1N NaOH. The organic layer was then dried and concentrated to give the product (1.38 g, 88%) as light yellow liquid. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 0.95 (t, J=7.6 Hz, 3 H) 1.31 (t, J=7.1 Hz, 4 H) 1.41-1.94 (m, 9 H) 2.88-3.08 (m, 3 H) 4.26 (qd, J=7.12, 2.40 Hz, 2 H). [M+H] calc'd for C12H22FNO2, 232; found 232.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318727B2
Source datasetuspto-grants-2012_11
ORD IDord-e4f6e835d6b2431a8253c7b65b283e45
Source noteuspto-grants-2012_11