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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914164Generated: November 2, 2026

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

https://huagongshe.com/reaction/914164

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, 3H) 1.31 (t, J=7.1 Hz, 4H) 1.41-1.94 (m, 9H) 2.88-3.08 (m, 3H) 4.26 (qd, J=7.12, 2.40 Hz, 2H). [M+H] calc'd for C12H22FNO2, 232. found 232.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026234B2
Source datasetuspto-grants-2011_09
ORD IDord-2c86a1b125e346099a8b9229b404ba34
Source noteuspto-grants-2011_09