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HRID 1839430Erstellt: 23. Oktober 2026

2-(3,4-Dichlorophenoxy)-5-fluorobenzaldehyde → 2-(3,4-Dichlorophenoxy)-5-fluoro-benzoic acid

https://huagongshe.com/de/reaction/1839430

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(3,4-Dichlorophenoxy)-5-fluorobenzaldehydeHCID 22019271—
EduktJones' reagentHCID 131709961—
LösungsmittelAcetoneHCID 180—
Produkt2-(3,4-Dichlorophenoxy)-5-fluoro-benzoic acidHCID 22019277—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

Alternatively, a solution of 4.28 g (15 mmol) of 2-(3,4-dichloro-phenoxy)-5-fluorobenzaldehyde (Preparation no. 5) in 25 mL of acetone was cooled to 5-10° C. and treated via syringe with 5.8 mL (15.6 mmol) of 2.67 M Jones reagent*. After 1 hr at this temperature, the reaction was quenched with 8 mL of isopropanol, allowed to warm to 25° C., and filtered through a pad of d.e. The filtrate was concentrated in vacuo to approximately ¼ volume, diluted with water and extracted several times with CHCl3. The organic layers were washed with water, then with saturated NaCl and finally dried over MgSO4 and concentrated to provide 2-(3,4-dichlorophenoxy)-5-fluoro-benzoic acid as a tan solid, 4.19 g. 1H-nmr (CDCl3, 400 MHz, δ): 7.78 (dd, 1H), 7.38 (d, 1H), 7.27 (m, 1H), 6.98 (m, 2H), 6.81 (dd, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06677378B2
Quelldatensatzuspto-grants-2004_01
ORD IDord-f72ff8a8272c46549f0fb40dbe2dd129
Quellennotizuspto-grants-2004_01