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HRID 1671378Erstellt: 26. Oktober 2026

Hydrochloric Acid → (S)-3-[(R)-1-(2,4,5-Trifluorophenoxy)pentyl]pyrrolidine

https://huagongshe.com/reaction/1671378

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthanolHCID 702—
EduktDimethylformamideHCID 6228—
Edukt1,2,4,5-TetrafluorobenzeneHCID 9474—
EduktSodium hydrideHCID 24758—
Edukt(S)-3-((R)-1-Hydroxypentyl)pyrrolidine-1-carboxylic acid t-butyl esterHCID 58104597—
Produkt(S)-3-[(R)-1-(2,4,5-Trifluorophenoxy)pentyl]pyrrolidineHCID 58104617—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

(S)-3-((R)-1-Hydroxypentyl)pyrrolidine-1-carboxylic acid t-butyl ester (40.0 mg, 155 μmmol) was dissolved in DMF (100 mL, 12.9 mmol). While stirring, 60% sodium hydride in oil (0.4:0.6, sodium hydride:mineral oil, 18.6 mg, 311 μmmol) was slowly added, and the mixture was stirred for 15 minutes. 1,2,4,5-Tetrafluorobenzene (52.1 μL, 466 μmmol) was added. The mixture was then heated at 90° C. for 3 hours. The reaction was quenched with MeOH (1 mL), and the solvent was removed under reduced pressure. 1.25M HCl in EtOH (2.0 mL, 2.5 mmol) was added, and the mixture was stirred overnight. The product was concentrated and purified by preparative HPLC to yield the title compound as a mono-TFA salt (19.2 mg, 97% purity). MS m/z: [M+H]+ calcd for C15H20F3NO, 288.15; found 288.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07994209B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-7484aea67ff1420eb6a0bba6e22a6750
Quellennotizuspto-grants-2011_08