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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490133Generated: October 25, 2026

Sodium Fluoride → tert-butyl(2R)-2-[(dimethylamino)carbonyl]-4-fluoropyrrolidine-1-carboxylate

https://huagongshe.com/reaction/490133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium FluorideHCID 5235—
ReactantPotassium CarbonateHCID 11430—
ReactantN,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamineHCID 136149—
ReactantTert-butyl (2R,4R)-2-(dimethylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylateHCID 58815374—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Producttert-butyl(2R)-2-[(dimethylamino)carbonyl]-4-fluoropyrrolidine-1-carboxylateHCID 69064202—

Reaction Steps

2.89 g of a mixture (approximately 3:1) of 1,1,2,3,3,3-hexafluoro-1-(diethylamino)propane and 1,2,3,3,3-pentafluoro-1-(diethylamino)-2-propene was added dropwise over a period of 10 minutes, and under ice cooling, to a suspension of 2.64 g of the compound obtained in step 6-1 and 545 mg of sodium fluoride in 26 mL of dichloromethane, after which the reaction mixture was stirred for 16 hours at room temperature. After this, 100 mL of a 5% potassium carbonate aqueous solution was added under ice cooling to the reaction solution, and the reaction mixture was stirred for 30 minutes at the same temperature. After liquid separation, the aqueous layer thus obtained was extracted with chloroform (30 mL×2), and the combined organic layer was washed with 50 mL of saturated brine and dried with magnesium sulfate, after which the drying agent was filtered off and the solvent was distilled off under reduced pressure. The residue thus obtained was subjected to column chromatography (silica gel 60, mobile phase: ethyl acetate) to obtain 2.17 g of the titled compound (colorless solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528124B2
Source datasetuspto-grants-2009_05
ORD IDord-338b936ee2b44320b924c4e3d66dcc28
Source noteuspto-grants-2009_05