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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410286Generated: November 2, 2026

Trifluoroacetic acid → 1-(3-(2-Fluoropyridin-3-yl)pyrrolidin-1-yl)ethanone

https://huagongshe.com/reaction/410286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 3-(2-fluoropyridin-3-yl)pyrrolidine-1-carboxylateHCID 59326787—
SolventDichloromethaneHCID 6344—
Product1-(3-(2-Fluoropyridin-3-yl)pyrrolidin-1-yl)ethanoneHCID 59327217—

Reaction Steps

To tert-butyl 3-(2-fluoropyridin-3-yl)pyrrolidine-1-carboxylate (0.25 g, 0.939 mmol) dissolved in DCM (3.1 mL) was added trifluoroacetic acid (1.05 mL, 14.1 mmol). The reaction mixture was stirred at RT for 1 h. The solvent was evaporated in vacuo and to the residue dissolved in DCM (1 mL) was added acetic anhydride (0.44 mL, 4.7 mmol) and sodium bicarbonate (0.4 g, 4.7 mmol). The reaction mixture was stirred at RT under N2 for 3 h. The reaction mixture was partitioned between 1N NaOH and DCM. The aqueous layer was back extracted with DCM (3×) and the combined DCM layer was dried (Na2SO4) and concentrated. The crude material was purified by chromatography through a Redi-Sep pre-packed silica gel column (40 g), eluting with a gradient of 0% to 100% EtOAc in hexane, then 10% MeOH in EtOAc, to provide 1-(3-(2-fluoropyridin-3-yl)pyrrolidin-1-yl)ethanone as tan oil. [M+H]=209.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759532B2
Source datasetuspto-grants-2014_06
ORD IDord-d715fcb687544b88a4e7586e6b26e712
Source noteuspto-grants-2014_06