HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-(3,4-Dichlorophenoxy)-5-fluorobenzaldehyde | HCID 22019271 | — |
| Edukt | Jones' reagent | HCID 131709961 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | 2-(3,4-Dichlorophenoxy)-5-fluoro-benzoic acid | HCID 22019277 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06677378B2 |
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| Quelldatensatz | uspto-grants-2004_01 |
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| ORD ID | ord-f72ff8a8272c46549f0fb40dbe2dd129 |
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| Quellennotiz | uspto-grants-2004_01 |
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