Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantCyanuric fluorideHCID 12664—
Reactant1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)-HCID 85083—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 2-(fluorocarbonyl)pyrrolidine-1-carboxylateHCID 14824272—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716236B2
Source datasetuspto-grants-2014_05
ORD IDord-b33449457fe1468096cbfce0f9b5e51a
Source noteuspto-grants-2014_05