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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 340850Erstellt: 25. Oktober 2026

3-Aminophenol → 3-Azidophenol

https://huagongshe.com/reaction/340850

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-AminophenolHCID 11568—
EduktSodium AzideHCID 33557—
EduktSodium NitriteHCID 23668193—
LösungsmittelHydrochloric AcidHCID 313—
Produkt3-AzidophenolHCID 1136701374,3%

Reaktionsschritte

An aqueous solution (15 mL) of NaNO2 (3.79 g, 54.98 mmol) was added dropwise to 3-aminophenol (5.0 g, 45 mmol) in 2 N HCl (100 mL) at 0-5° C. The solution was stirred for 30 minutes, followed by addition of an aqueous solution of sodium azide (4.5 g, 69 mmol, in 35 mL water). The mixture was stirred at room temperature for 24 h, and extracted with 300 mL of ethyl acetate. The combined organic layer was washed with water, and dried over MgSO4. Solvents were removed by rotary evaporation, and the residue was purified by column chromatography (EtOAc/hexanes, 1/4) to give the desired product as a dark red oil (4.52 g, 73% yield): 1H NMR (acetone-d6, 300 MHz, ppm): 8.69 (s, 1H, Ar—OH), 7.24 (t, 1H, J=8.1 Hz, Ar—H), 6.70-6.53 (m, 3H, Ar—H). 13C NMR (CDCl3, 75 MHz, ppm): 157.2, 141.6, 130.9, 112.4, 111.5, 106.5. FT-IR (cm−1): 3348, 2109.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895688B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-52ac7e7cc7b149b2a99c80a26b7884cd
Quellennotizuspto-grants-2014_11