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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | tert-Butyl 4-[(azetidin-1-yl)carbonyl]piperidine-1-carboxylate | HCID 23658779 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Azetidine-1-carbonyl)piperidine | HCID 23658780 | 102.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106208B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-0a8d6dea2fee4d158928244235de5d67 |
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| Source note | uspto-grants-2012_01 |
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