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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 918608Erstellt: 25. Oktober 2026

3-Chlorophenol → 4-(m-Chlorophenoxy)-3-nitro-5-sulphamyl-benzoic acid

https://huagongshe.com/reaction/918608

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-ChlorophenolHCID 7933—
Edukt4-Chloro-3-nitro-5-sulphamoylbenzoic acidHCID 89893—
EduktSodium BicarbonateHCID 516892—
LösungsmittelWaterHCID 962—
Produkt4-(m-Chlorophenoxy)-3-nitro-5-sulphamyl-benzoic acidHCID 21506084—

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

A mixture of 4-chloro-3-nitro-5-sulphamyl-benzoic acid (28 g), m-chlorophenol (26 g), sodium bicarbonate (34 g), and water (200 ml) was stirred at 85°C for 10 hours. After cooling, excess m-chlorophenol was removed by extraction with diethyl ether, and 4-(m-chlorophenoxy)-3-nitro-5-sulphamyl-benzoic acid was precipitated from the aqueous layer by the addition of 4N hydrochloric acid. After recrystallization from aqueous methanol, the melting point was 230°-232°C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03971819
Quelldatensatzuspto-grants-1976_07
ORD IDord-45f881ade9bd44aab588515e535601a0
Quellennotizuspto-grants-1976_07