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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 490119Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/490119

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium FluorideHCID 5235—
EduktPotassium CarbonateHCID 11430—
EduktN,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamineHCID 136149—
Edukt(2S,4R)-tert-butyl 2-(dimethylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylateHCID 25180889—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl acetate hexaneHCID 21226206—
Produkttert-butyl(2S,4R)-2-[(dimethylamino)carbonyl]-4-fluoropyrrolidine-1-carboxylateHCID 67428750—

Reaktionsschritte

26.6 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 under ice cooling to a suspension of 25.7 g of the compound obtained in step 1-1a and 5.00 g of sodium fluoride in 260 mL of dichloromethane, after which the reaction mixture was stirred for 16 hours at room temperature. 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, 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/n-hexane=1/1 to 10/0; v/v) to obtain 12.2 g of the titled compound (pale yellow solid).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07528124B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-7a5cfd9f7de94b12a9f824563214f085
Quellennotizuspto-grants-2009_05