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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 380613Erstellt: 25. Oktober 2026

Ethyl Acetate → 7-Bromo-5-nitrobenzothiazole

https://huagongshe.com/reaction/380613

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktNitrosylsulfuric acidHCID 82157—
EduktPhosphinic AcidHCID 4124402—
Edukt7-Bromo-5-nitrobenzo[d]thiazol-6-amineHCID 22728034—
LösungsmittelSulfuric AcidHCID 1118—
Produkt7-Bromo-5-nitrobenzothiazoleHCID 2272803189%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

To a solution of 5-nitro-6-amino-7-bromobenzothiazole (1.0 g, 3.7 mmol) in 4 mL of sulfuric acid was added nitrososulfuric acid (1.2 g, 9.5 mmol) in a portion. The resulting reaction mixture was stirred for 12 h at 25° C. The reaction mixture was then cooled to 0° C. and 1 mL of H3PO2 was added into the solution. It was stirred for 12 h at another 25° C. and for 2 h at 50° C. The reaction mixture was then poured into EtOAc and washed with aq. NaHCO3. Organic layer was dried over Na2SO4 and concentrated in vacuo to provide an oil (0.85 g, 3.2 mmol, 89%), which was characterized as the desired product(>95% pure) and subjected to a following reaction without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06303643B1
Quelldatensatzuspto-grants-2001_10
ORD IDord-c3011ab581014581b8ca55f3bfe37049
Quellennotizuspto-grants-2001_10