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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1931824Erstellt: 26. Oktober 2026

Iodoethane → 3-(3-Chloro-2-fluorophenyl)-1-ethylpyrrolidin-3-ol

https://huagongshe.com/reaction/1931824

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodoethaneHCID 6340—
Edukt1-Benzyl-3-(3-chloro-2-fluorophenyl)pyrrolidin-3-olHCID 68515790—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(3-Chloro-2-fluorophenyl)-1-ethylpyrrolidin-3-olHCID 2514367053,2%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

In a sealed tube a mixture of (+)-1-benzyl-3-(3-chloro-2-fluorophenyl)pyrrolidin-3-ol (0.31 g, 1.01 mmol), dimethyl formamide (3 mL) and iodoethane (0.16 mL, 2.02 mmol) was heated under microwave irradiation at 80° C. for 2×15 minutes. The resulting mixture was evaporated, morpholine (2 mL) was added and the mixture was heated under microwave irradiation at 130° C. for 30 minutes. Aqueous LiCl (5%, 50 mL) was added and the aqueous phase was extracted with ethyl acetate (2×50 mL, dried (Na2SO4) and evaporated. Purification by flash chromatography on silica gel (ethyl acetate/methanol, 1:0 to 1:1) gave the title compound (0.131 g). [α]D=+27.2° (methanol). The amine was converted to the oxalic acid salt and recrystallized from methanol/diethyl ether/diisopropyl ether: M.p. 71-74° C.; MS m/z (relative intensity, 70 eV) 243 (M+, 13), 228, (10), 157 (12), 72 (26), 71 (bp).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08188301B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-0e167ac8dc164994929fbf3e11ab8bc4
Quellennotizuspto-grants-2012_05