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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 458086Erstellt: 23. Oktober 2026

2-Bromo-4-nitroanisole → 2-Bromo-4-nitrophenol

https://huagongshe.com/de/reaction/458086

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromo-4-nitroanisoleHCID 78870—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-Bromo-4-nitrophenolHCID 2210952,3%

Reaktionsbedingungen

Temperatur115 °C

Reaktionsschritte

2-Bromo4-nitroanisole (20 g, 0.086 mol) was dissolved in DMF (414 mL) at rt under N2. Sodium ethylthiolate (17.4 g, 0.207 mol) was added and the reaction mixture was warmed to 115° C. for 2 h. The reaction was cooled to rt and diluted with EtOAc (200 mL) and 1 M HCl (aq., 200 mL). The phases were separated, and the desired product was extracted into 1 M NaOH (aq, 150 mL×3). The basic aqueous extracts were combined and acidified using conc. HCl. The desired product was extracted from the acidic aqueous solution using EtOAc (250 mL×2). The combined organic layers were washed with brine and dried over sodium sulfate. The volatiles were removed in vacuo to afford a light brown semi-solid (9.8 g, 52% yield). 1H NMR (DMSO-d6) δ 8.33 (m, 1H); 8.09 (m, 1H); 7.07 (d, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07189734B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-8c964f0ad2554b1996530ab96f95cdac
Quellennotizuspto-grants-2007_03