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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426084Generated: November 1, 2026

Trifluoroacetic acid → 4-(Azetidine-1-carbonyl)piperidine

https://huagongshe.com/reaction/426084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl 4-[(azetidin-1-yl)carbonyl]piperidine-1-carboxylateHCID 23658779—
SolventDichloromethaneHCID 6344—
Product4-(Azetidine-1-carbonyl)piperidineHCID 23658780102.3%

Reaction Steps

tert-Butyl 4-(azetidin-1-ylcarbonyl)piperidine-1-carboxylate (0.50 g, 1.86 mmol) was dissolved in methylene chloride (10 mL) and to the solution was added trifluoroacetic acid (2.12 g, 18.6 mmol). The mixture was stirred at RT overnight and then the solvent was removed by evaporation. The residue was dissolved in a small amount of methanol and THF and the solution was then loaded on a cation exchange sorbent (Isolute® SCX-2; 10 g). The column washed with THF and the product was then eluted with ammonia saturated methanol. The solvent was removed by evaporation. There was obtained 0.32 g (100%) of 4-(azetidin-1-ylcarbonyl)piperidine. 1H NMR (500 MHz, CDCl3): 1.4-1.5 (m, 4H), 2.0-2.2 (m, 3H), 2.4-2.5 (m, 2H), 2.9-3.0 (d, 2H), 3.7-3.8 (t, 2H), 3.9 (s, 1H), 4.0 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106208B2
Source datasetuspto-grants-2012_01
ORD IDord-0a8d6dea2fee4d158928244235de5d67
Source noteuspto-grants-2012_01