Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 472015Erstellt: 24. Oktober 2026

Dimethylformamide → 3-Fluoro-4-nitrobenzoyl chloride

https://huagongshe.com/de/reaction/472015

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktThionyl ChlorideHCID 24386—
Edukt3-Fluoro-4-nitrobenzoic acidHCID 230653—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Fluoro-4-nitrobenzoyl chlorideHCID 2774656—

Reaktionsschritte

To a solution of 3-fluoro-4-nitrobenzene carboxylic acid (18.0 g 1.0 eq, 0.10 mol) in THF (360 ml) at 0° C. was added thionyl chloride (56.7 ml, 8.0 eq, 0.78 mol) and DMF (1 ml.). The reaction was warmed to room temperature and stirred for 3.5 hours, after this point all starting material had been consumed. Thionyl chloride was then removed in vacuo to give 3-fluoro-4-nitrobenzoyl chloride as a yellow solid. This was dissolved in DCM (360 ml) and the solution added dropwise to a cooled solution of 880 ammonia in water (360 ml) with vigorous stirring. After the addition the reaction was stirred at room temperature for 15 minutes. The resultant precipitate was collected by filtration, and the filtrate was then filtered a further two more times. The three precipitates were each washed with cyclohexane (2×100 ml), dried in vacuo and combined to give the title compound as a yellow solid (13.32 g, 72 mmol, 74%). LCMS: [M+H]+=na, Rt=1.41 min, 100% purity.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08633201B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-e92d8cfeccd343e898a5369edcd8e0c6
Quellennotizuspto-grants-2014_01