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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 490121Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/490121

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium FluorideHCID 5235—
EduktN,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamineHCID 136149—
EduktSodium BicarbonateHCID 516892—
Edukttert-butyl (2S,4S)-2-(dimethylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylateHCID 67430109—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl acetate hexaneHCID 21226206—
Produkttert-butyl(2S,4R)-2-[(dimethylamino)carbonyl]-4-fluoropyrrolidine-1-carboxylateHCID 67428750—

Reaktionsschritte

8.85 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 2 minutes under ice cooling to a suspension of 8.54 g of the compound obtained in step 1-1b and 1.67 g of sodium fluoride in 90 mL of dichloromethane, after which the reaction mixture was stirred for 15 hours at room temperature. 200 mL of a saturated sodium hydrogencarbonate aqueous solution was added dropwise to the reaction solution over a period of 3 minutes, and the reaction mixture was stirred for 1 hour. After liquid separation, the aqueous layer 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 reaction mixture was concentrated under reduced pressure. The residue thus obtained was subjected to column chromatography (silica gel 60, mobile phase: ethyl acetate/n-hexane=1/1 to 10/0; v/v) to obtain 7.54 g of the titled compound (pale yellow solid).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07528124B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-4b4ebc80d4454c65a2ab4a904986eab6
Quellennotizuspto-grants-2009_05