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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880149Generated: October 25, 2026

Trifluoroacetic acid → 1-(2-(2-Fluoropyridin-3-YL)piperidin-1-YL)ethanone

https://huagongshe.com/reaction/1880149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAcetic AnhydrideHCID 7918—
ReactantTert-butyl 2-(2-fluoropyridin-3-yl)piperidine-1-carboxylateHCID 59327149—
SolventDichloromethaneHCID 6344—
Product1-(2-(2-Fluoropyridin-3-YL)piperidin-1-YL)ethanoneHCID 59326960—

Reaction Steps

To a solution of tert-butyl 2-(2-fluoropyridin-3-yl)piperidine-1-carboxylate (70 mg, 0.250 mmol) and DCM (5 mL) was added TFA (0.50 mL, 6.49 mmol). After 1 hour, the reaction was washed with 10% Na2CO3. The organic layer was treated with TEA (0.070 mL, 0.499 mmol), then acetic anhydride (0.024 mL, 0.250 mmol). After 15 minutes, LC-MS shows conversion to the desired product [M+1=223]. The reaction was washed with water and concentrated in vacuo to give 1-(2-(2-fluoropyridin-3-yl)piperidin-1-yl)ethanone as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318718B2
Source datasetuspto-grants-2012_11
ORD IDord-305bb6f258184b1bb0283be2d31bd7bd
Source noteuspto-grants-2012_11