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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809948Generated: October 31, 2026

Trifluoroacetic acid → HCID 54443836, compound

https://huagongshe.com/reaction/1809948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBenzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 2-(fluoromethyl)prop-2-enoateHCID 12815505—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 54443836HCID 5444383623%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of N-benzyl-1-methoxy-N-[(trimethylsilyl)methyl]methanamine (2.5 g, 21 mmol) and ethyl 2-(fluoromethyl)acrylate (5.0 g, 21 mmol) in methylene chloride (30 mL) was added TFA (0.15 ml, 2.1 mmol) at 0° C. The reaction mixture was stirred at 0° C. overnight. 20 mL of saturated NaHCO3 aqueous solution and 20 mL of ethyl acetate were added to quench the reaction. The organic layer was separated, and the aqueous layer was extracted twice with EtOAc (20 mL×2). The combined organic extracts were dried over MgSO4 and evaporated to give an oil residue. Chromatography on silica gel with 10% EtOAc-Hexane afforded 1.27 g (4.8 mmol, yield: 23%) of ethyl 1-benzyl-3-(fluoromethyl)pyrrolidine-3-carboxylate: 1H NMR (400 MHz, CDCl3) δ 7.39-7.20 (5H, m), 4.62-4.44 (2H, m), 4.18-4.21 (2H, m), 3.62 (2H, s), 2.81-2.72 (2H, m), 2.60-2.50 (2H, m), 2.22 (2H, s), 1.25 (3H, t, J=6.7 Hz); MS (m/e): 266 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362003B2
Source datasetuspto-grants-2013_01
ORD IDord-fc94d836bbc443ebbefe2df273be58de
Source noteuspto-grants-2013_01