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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37831Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-Chloro-5-nitrophenol

https://huagongshe.com/de/reaction/37831

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthyl AcetateHCID 8857—
Edukt2-Amino-5-NitrophenolHCID 4984721—
EduktSodium NitriteHCID 23668193—
KatalysatorCuprous chlorideHCID 62652—
LösungsmittelWaterHCID 962—
Produkt2-Chloro-5-nitrophenolHCID 6926492%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A saturated solution of sodium nitrite (1.8 g, 26.0 mmol) in water (12 mL) was added dropwise to a suspension of 2-amino-5-nitro-phenol (2.0 g, 13.0 mmol) in concentrated hydrochloric acid (10 mL) at 0° C. and stirred for 30 min. In another flask, copper (I) chloride (5.15 g, 52.0 mmol) and concentrated hydrochloric acid (20 mL) were heated to between 60 and 70° C. and the diazonium salt solution was added dropwise to this over a period of 30 min. The reaction mixture was heated to 80° C. and stirred for 15 min. It was then cooled to room temperature and ethyl acetate (50 mL) was added and stirred for 5 min. The organic phase was separated and the aqueous phase was extracted with ethyl acetate (2×50 mL). The combined organic phases were washed with water (4×50 mL), brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give a residue which was purified by column chromatography over silica gel (100-200 mesh) using 5% ethyl acetate in petroleum ether as eluent to afford 2-chloro-5-nitro-phenol (2.08 g, 92%) as a crystalline yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524705B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-d638fc1dd9e949e4bf025e357cbd4d69
Quellennotizuspto-grants-2013_09