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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 370069Erstellt: 24. Oktober 2026

5-Chloro-2-nitrobenzoic acid → 5-Chloro-2-nitrobenzoyl chloride

https://huagongshe.com/de/reaction/370069

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Chloro-2-nitrobenzoic acidHCID 17286—
EduktOxalyl chlorideHCID 65578—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-Chloro-2-nitrobenzoyl chlorideHCID 2723685104,5%

Reaktionsschritte

To a suspension of 5-chloro-2-nitrobenzoic acid (21 g, 100 mmol) in dry methylene chloride (200 mL) at 0° C. were added several drops of DMF, followed by oxalyl chloride (13 mL, 150 mmol). The reaction was warmed to ambient temperature. After 16 hours the solvents were removed and the viscous oil dried in vacuo to afford 23 g (quantitative yield) of 5-chloro-2-nitrobenzoyl chloride; NMR (CDCl3) 8.1 (d, 1), 7.7 (m, 2) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06140351
Quelldatensatzuspto-grants-2000_10
ORD IDord-334ab236062a4121888a04ebcb61115d
Quellennotizuspto-grants-2000_10