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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 370070Erstellt: 25. Oktober 2026

4-Chloroaniline → Benzamide, 5-chloro-N-(4-chlorophenyl)-2-nitro-

https://huagongshe.com/reaction/370070

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-ChloroanilineHCID 7812—
EduktTriethylamineHCID 8471—
Edukt5-Chloro-2-nitrobenzoyl chlorideHCID 2723685—
LösungsmittelDichloromethaneHCID 6344—
ProduktBenzamide, 5-chloro-N-(4-chlorophenyl)-2-nitro-HCID 87378896,4%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 5-chloro-2-nitrobenzoyl chloride (23 g, 100 mmol) in methylene chloride (200 mL) at 0° C. was added triethylamine (16 mL, 115 mmol), followed by 4-chloroaniline (14 g, 110 mmol). The mixture was stirred for 20 minutes at 0° C., then warmed to ambient temperature. After 5 hours, the mixture was concentrated of all volatiles in vacuo. The residual solid was dissolved in ethyl acetate (400 mL) and washed with water (200 mL), 1M hydrochloric acid (2×200 mL), 1M sodium bicarbonate (200 mL) and brine (200 mL) and dried over MgSO4. Concentration and drying in vacuo afforded 30 g (93% yield) of N-(4-chlorophenyl)-5-chloro-2-nitrobenzamide; NMR (CDCl3) 8.1 (d, 1), 7.7 (br, 1), 7.6 (m, 2), 7.5 (d, 2), 7.3 (d, 2) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06140351
Quelldatensatzuspto-grants-2000_10
ORD IDord-f4c5f35d2823493db635c085dca346c8
Quellennotizuspto-grants-2000_10