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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40316Erstellt: 23. Oktober 2026

2-(Quinolin-6-yl)propanoic acid → 2-Fluoro-2-(quinolin-6-yl)propanoic acid

https://huagongshe.com/de/reaction/40316

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Quinolin-6-yl)propanoic acidHCID 19036006—
EduktMethyl 2-fluoro-2-(quinolin-6-yl)propanoateHCID 67503402—
Produkt2-Fluoro-2-(quinolin-6-yl)propanoic acidHCID 57691062—

Reaktionsschritte

To a solution of methyl 2-(quinolin-6-yl)propanoate (0.868 g, 4.03 mmol) in THF (1.1M, 3.7 mL) at −78° C. was added LiHMDS (1M in THF) (5.24 ml, 5.24 mmol). The reaction was stirred at −78° C. for ˜15 minutes, then to it was added a solution of N-fluorobenzenesulfonimide (1.40 g, 4.44 mmol) in THF (1.0M, 4.5 mL). The reaction was allowed to warm to −10° C. over 2 h. The reaction was filtered through a plug of Celite, washed with EtOAc and the filtrate was then concentrated in vacuo. The concentrated material was rediluted with EtOAc and washed with saturated NH4Cl solution. The aqueous layer was then extracted with EtOAc, and the organic layers were dried over MgSO4, filtered and concentrated in vacuo. The crude material was dissolved in minimal DCM and purified via MPLC (eluting with isocratic 40% EtOAc:Hexanes to yield methyl 2-fluoro-2-(quinolin-6-yl)propanoate (0.709 g, 75.4% yield) as a yellow oil. To synthesize the corresponding acid, methyl 2-fluoro-2-(quinolin-6-yl)propanoate was saponified in a method similar to that of 2-(quinolin-6-yl)propanoic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524900B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-82114ff7e3584801b7f5753c8f1a9749
Quellennotizuspto-grants-2013_09