HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019513Generated: October 30, 2026
Pyridine → Tert-butyl 2-(fluorocarbonyl)pyrrolidine-1-carboxylate
https://huagongshe.com/reaction/1019513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Cyanuric fluoride | HCID 12664 | — |
| Reactant | 1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)- | HCID 85083 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 2-(fluorocarbonyl)pyrrolidine-1-carboxylate | HCID 14824272 | — |
Reaction Steps
To a solution of Boc-L-Proline (4.5 g, 0.02 mmol) and pyridine (8.45 mL, 0.104 mmol) in DCM (20 mL) cooled in an ice bath was added dropwise cyanuric fluoride (5.35 mL, 0.0627 mmol). After the addition the reaction became milky. The solution was stirred at 0° C. for 10 min then warmed to RT and stirred for 4 h. The reaction was quenched with water, and thrice extracted with DCM. The combined organic extracts were washed with brine, dried, and concentrated in vacuo to afford tert-butyl 2-(fluorocarbonyl)pyrrolidine-1-carboxylate. The crude acid fluoride was used in next coupling reaction immediately.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716236B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-b33449457fe1468096cbfce0f9b5e51a |
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| Source note | uspto-grants-2014_05 |
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