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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 416614Erstellt: 24. Oktober 2026

2-Bromo-2'-nitroacetophenone → 4-(2-Nitrophenyl)thiazole-2-amine

https://huagongshe.com/de/reaction/416614

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromo-2'-nitroacetophenoneHCID 244025—
EduktThioureaHCID 2723790—
LösungsmittelEthanolHCID 702—
Produkt4-(2-Nitrophenyl)thiazole-2-amineHCID 595779—

Reaktionsschritte

4-(2-Nitro-phenyl)-thiazol-2-ylamine was prepared as follows: 2-Bromo-2′-nitroacetophenone (1.75 g, 7.2 mmol) was mixed with 50 mL of absolute EtOH along with thiourea (1.09 g, 14.4 mmol) and stirred under reflux for 2 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The resulting residue was basified with 20 mL of 1 N aqueous NaOH and extracted with CH2Cl2. The combined organic layers were dried (Na2SO4) and concentrated to afford essentially quantitative yield of 4-(2-nitro-phenyl)-thiazol-2-ylamine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08088928B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-f45d86eaa3234b0bbb13b75f84f29e24
Quellennotizuspto-grants-2012_01